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Prenol: Chemical Properties and Applications

At a Glance

Title: Prenol: Chemical Properties and Applications

Total Categories: 5

Category Stats

  • Chemical Identity and Structure: 18 flashcards, 18 questions
  • Physical Properties: 9 flashcards, 12 questions
  • Safety and Hazard Classification: 4 flashcards, 8 questions
  • Industrial Production and Applications: 7 flashcards, 9 questions
  • Natural Occurrence and Biological Context: 10 flashcards, 9 questions

Total Stats

  • Total Flashcards: 48
  • True/False Questions: 30
  • Multiple Choice Questions: 26
  • Total Questions: 56

Instructions

Click the button to expand the instructions for how to use the Wiki2Web Teacher studio in order to print, edit, and export data about Prenol: Chemical Properties and Applications

Welcome to Your Curriculum Command Center

This guide will turn you into a Wiki2web Studio power user. Let's unlock the features designed to give you back your weekends.

The Core Concept: What is a "Kit"?

Think of a Kit as your all-in-one digital lesson plan. It's a single, portable file that contains every piece of content for a topic: your subject categories, a central image, all your flashcards, and all your questions. The true power of the Studio is speed—once a kit is made (or you import one), you are just minutes away from printing an entire set of coursework.

Getting Started is Simple:

  • Create New Kit: Start with a clean slate. Perfect for a brand-new lesson idea.
  • Import & Edit Existing Kit: Load a .json kit file from your computer to continue your work or to modify a kit created by a colleague.
  • Restore Session: The Studio automatically saves your progress in your browser. If you get interrupted, you can restore your unsaved work with one click.

Step 1: Laying the Foundation (The Authoring Tools)

This is where you build the core knowledge of your Kit. Use the left-side navigation panel to switch between these powerful authoring modules.

⚙️ Kit Manager: Your Kit's Identity

This is the high-level control panel for your project.

  • Kit Name: Give your Kit a clear title. This will appear on all your printed materials.
  • Master Image: Upload a custom cover image for your Kit. This is essential for giving your content a professional visual identity, and it's used as the main graphic when you export your Kit as an interactive game.
  • Topics: Create the structure for your lesson. Add topics like "Chapter 1," "Vocabulary," or "Key Formulas." All flashcards and questions will be organized under these topics.

🃏 Flashcard Author: Building the Knowledge Blocks

Flashcards are the fundamental concepts of your Kit. Create them here to define terms, list facts, or pose simple questions.

  • Click "➕ Add New Flashcard" to open the editor.
  • Fill in the term/question and the definition/answer.
  • Assign the flashcard to one of your pre-defined topics.
  • To edit or remove a flashcard, simply use the ✏️ (Edit) or ❌ (Delete) icons next to any entry in the list.

✍️ Question Author: Assessing Understanding

Create a bank of questions to test knowledge. These questions are the engine for your worksheets and exams.

  • Click "➕ Add New Question".
  • Choose a Type: True/False for quick checks or Multiple Choice for more complex assessments.
  • To edit an existing question, click the ✏️ icon. You can change the question text, options, correct answer, and explanation at any time.
  • The Explanation field is a powerful tool: the text you enter here will automatically appear on the teacher's answer key and on the Smart Study Guide, providing instant feedback.

🔗 Intelligent Mapper: The Smart Connection

This is the secret sauce of the Studio. The Mapper transforms your content from a simple list into an interconnected web of knowledge, automating the creation of amazing study guides.

  • Step 1: Select a question from the list on the left.
  • Step 2: In the right panel, click on every flashcard that contains a concept required to answer that question. They will turn green, indicating a successful link.
  • The Payoff: When you generate a Smart Study Guide, these linked flashcards will automatically appear under each question as "Related Concepts."

Step 2: The Magic (The Generator Suite)

You've built your content. Now, with a few clicks, turn it into a full suite of professional, ready-to-use materials. What used to take hours of formatting and copying-and-pasting can now be done in seconds.

🎓 Smart Study Guide Maker

Instantly create the ultimate review document. It combines your questions, the correct answers, your detailed explanations, and all the "Related Concepts" you linked in the Mapper into one cohesive, printable guide.

📝 Worksheet & 📄 Exam Builder

Generate unique assessments every time. The questions and multiple-choice options are randomized automatically. Simply select your topics, choose how many questions you need, and generate:

  • A Student Version, clean and ready for quizzing.
  • A Teacher Version, complete with a detailed answer key and the explanations you wrote.

🖨️ Flashcard Printer

Forget wrestling with table layouts in a word processor. Select a topic, choose a cards-per-page layout, and instantly generate perfectly formatted, print-ready flashcard sheets.

Step 3: Saving and Collaborating

  • 💾 Export & Save Kit: This is your primary save function. It downloads the entire Kit (content, images, and all) to your computer as a single .json file. Use this to create permanent backups and share your work with others.
  • ➕ Import & Merge Kit: Combine your work. You can merge a colleague's Kit into your own or combine two of your lessons into a larger review Kit.

You're now ready to reclaim your time.

You're not just a teacher; you're a curriculum designer, and this is your Studio.

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Text content is available under the Creative Commons Attribution-ShareAlike 4.0 License (opens in new tab). Additional terms may apply.

Disclaimer: This website is for informational purposes only and does not constitute any kind of advice. The information is not a substitute for consulting official sources or records or seeking advice from qualified professionals.


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Study Guide: Prenol: Chemical Properties and Applications

Study Guide: Prenol: Chemical Properties and Applications

Chemical Identity and Structure

The preferred IUPAC name for Prenol is 3,3-Dimethylallyl alcohol.

Answer: False

The preferred IUPAC name for Prenol is 3-Methylbut-2-en-1-ol. While 3,3-Dimethylallyl alcohol is a common name, it is not the systematic IUPAC designation.

Related Concepts:

  • What are some common names used for Prenol?: Besides its preferred IUPAC name, Prenol is also commonly known as 3,3-Dimethylallyl alcohol. These alternative names are frequently encountered in scientific literature and industrial contexts.
  • What is the preferred IUPAC nomenclature for Prenol?: The preferred IUPAC nomenclature for Prenol is 3-Methylbut-2-en-1-ol. Adherence to IUPAC nomenclature ensures systematic and unambiguous identification of chemical compounds within the scientific community.
  • What is Prenol's identifier on the ChemSpider database?: Prenol is identified by the number 10700 on ChemSpider, a comprehensive chemical database that provides access to information regarding chemical structures and properties.

The CAS Registry Number assigned to Prenol is 10700.

Answer: False

The correct CAS Registry Number for Prenol is 556-82-1. The number 10700 is its identifier on the ChemSpider database.

Related Concepts:

  • What is the CAS Registry Number assigned to Prenol?: The CAS Registry Number for Prenol is 556-82-1. This unique numerical identifier, assigned by the Chemical Abstracts Service, is crucial for precise identification across databases and literature.
  • What is Prenol's identifier on the ChemSpider database?: Prenol is identified by the number 10700 on ChemSpider, a comprehensive chemical database that provides access to information regarding chemical structures and properties.
  • What is the PubChem Compound ID (CID) for Prenol?: The PubChem Compound ID for Prenol is 11173. PubChem is a widely used database for chemical molecules and their associated activities, and this CID allows for precise retrieval of Prenol's data.

Prenol has a molar mass of approximately 50 g/mol.

Answer: False

The molar mass of Prenol is approximately 86.132 g/mol. A value of 50 g/mol is significantly inaccurate.

Related Concepts:

  • What is the molar mass of Prenol?: The molar mass of Prenol is 86.132 g/mol. This fundamental property is essential for quantitative chemical analysis and calculations.
  • What is Prenol's identifier on the ChemSpider database?: Prenol is identified by the number 10700 on ChemSpider, a comprehensive chemical database that provides access to information regarding chemical structures and properties.
  • How soluble is Prenol in water?: Prenol exhibits a solubility of 17 grams per 100 milliliters in water at 20 °C. This indicates moderate solubility, meaning a significant amount can dissolve.

Oxidation of Prenol yields the ketone known as prenone.

Answer: False

Oxidation of Prenol yields the aldehyde known as prenal, not the ketone prenone. Prenal is an intermediate in the synthesis pathway towards citral.

Related Concepts:

  • What aldehyde is produced when Prenol is oxidized?: When Prenol is oxidized, it produces the aldehyde known as prenal. This aldehyde is a key step in the pathway to synthesizing citral.
  • What is the industrial process for producing Prenol?: Industrially, Prenol is produced by reacting formaldehyde with isobutene to form isoprenol (3-methyl-3-buten-1-ol), which is then isomerized to yield Prenol (3-methyl-2-buten-1-ol).
  • How does Prenol relate to the concept of 'isoprenols'?: Prenol is considered one of the simplest terpenoids and is a building block for isoprenoid alcohols, which are sometimes referred to as 'isoprenols' due to their structural relation to isoprene units. However, it is important not to confuse Prenol with its isomer, isoprenol (3-methyl-3-buten-1-ol).

Prenol has a unique identifier assigned by the European Chemicals Agency (ECHA) called an EC Number.

Answer: True

Prenol is assigned an EC Number (European Community number) of 209-141-4 by the European Chemicals Agency (ECHA), serving as a regulatory identifier within the EU.

Related Concepts:

  • What is Prenol's EC Number?: Prenol possesses an EC Number of 209-141-4. This number is assigned by the European Commission to uniquely identify chemical substances within the European market.
  • What is the ECHA InfoCard number for Prenol?: The ECHA (European Chemicals Agency) InfoCard number for Prenol is 100.008.312. This identifier serves as a gateway to regulatory information pertaining to the substance within the European Union.
  • What is the CAS Registry Number assigned to Prenol?: The CAS Registry Number for Prenol is 556-82-1. This unique numerical identifier, assigned by the Chemical Abstracts Service, is crucial for precise identification across databases and literature.

The SMILES string for Prenol is OC\C=C(/C)C.

Answer: True

The Simplified Molecular Input Line Entry System (SMILES) string OC\C=C(/C)C accurately represents the chemical structure of Prenol.

Related Concepts:

  • What is the SMILES string for Prenol?: The SMILES (Simplified Molecular Input Line Entry System) string for Prenol is OC\C=C(/C)C. SMILES offers a concise, ASCII-based method for representing chemical structures.
  • What is the standard InChI representation of Prenol?: The standard InChI (International Chemical Identifier) for Prenol is InChI=1S/C5H10O/c1-5(2)3-4-6/h3,6H,4H2,1-2H3, with the corresponding key being ASUAYTHWZCLXAN-UHFFFAOYSA-N. InChI provides a canonical textual representation of chemical structures.
  • What is Prenol's identifier on the ChemSpider database?: Prenol is identified by the number 10700 on ChemSpider, a comprehensive chemical database that provides access to information regarding chemical structures and properties.

The PubChem Compound ID (CID) for Prenol is CHEBI:16019.

Answer: False

The PubChem Compound ID (CID) for Prenol is 11173. CHEBI:16019 is its identifier in the ChEBI database.

Related Concepts:

  • What is the ChEBI identifier for Prenol?: The ChEBI (Chemical Entities of Biological Interest) identifier for Prenol is CHEBI:16019. This designation is utilized in biological and chemical databases for referencing the compound.
  • What is the PubChem Compound ID (CID) for Prenol?: The PubChem Compound ID for Prenol is 11173. PubChem is a widely used database for chemical molecules and their associated activities, and this CID allows for precise retrieval of Prenol's data.
  • What is Prenol's identifier on the ChemSpider database?: Prenol is identified by the number 10700 on ChemSpider, a comprehensive chemical database that provides access to information regarding chemical structures and properties.

The InChI key for Prenol is ASUAYTHWZCLXAN-UHFFFAOYSA-N.

Answer: True

The standard InChI key associated with Prenol is indeed ASUAYTHWZCLXAN-UHFFFAOYSA-N, providing a unique textual identifier for its structure.

Related Concepts:

  • What is the standard InChI representation of Prenol?: The standard InChI (International Chemical Identifier) for Prenol is InChI=1S/C5H10O/c1-5(2)3-4-6/h3,6H,4H2,1-2H3, with the corresponding key being ASUAYTHWZCLXAN-UHFFFAOYSA-N. InChI provides a canonical textual representation of chemical structures.
  • What is Prenol's identifier on the ChemSpider database?: Prenol is identified by the number 10700 on ChemSpider, a comprehensive chemical database that provides access to information regarding chemical structures and properties.
  • What is the ChEBI identifier for Prenol?: The ChEBI (Chemical Entities of Biological Interest) identifier for Prenol is CHEBI:16019. This designation is utilized in biological and chemical databases for referencing the compound.

Prenol contains 5 carbon atoms, 10 hydrogen atoms, and 1 oxygen atom per molecule.

Answer: True

The chemical formula for Prenol is C5H10O, confirming the presence of 5 carbon atoms, 10 hydrogen atoms, and 1 oxygen atom per molecule.

Related Concepts:

  • What is the chemical formula for Prenol?: The chemical formula for Prenol is C5H10O. This formula indicates that each molecule of Prenol comprises 5 carbon atoms, 10 hydrogen atoms, and 1 oxygen atom.
  • What does the image labeled 'Skeletal formula of prenol' depict?: The image labeled 'Skeletal formula of prenol' displays a simplified representation of the Prenol molecule's chemical structure, showing the arrangement of carbon and oxygen atoms and their bonds without explicitly drawing all hydrogen atoms.
  • What is Prenol's identifier on the ChemSpider database?: Prenol is identified by the number 10700 on ChemSpider, a comprehensive chemical database that provides access to information regarding chemical structures and properties.

Prenol can be visualized using an interactive 3D model accessible via JSmol.

Answer: True

The source material indicates that an interactive 3D model of Prenol is available for visualization through the JSmol platform.

Related Concepts:

  • Where can one access an interactive 3D model of Prenol?: An interactive 3D model of Prenol is accessible through the JSmol platform, providing a dynamic visualization of its molecular structure.
  • What information is conveyed by the 'Ball-and-stick model' image of Prenol?: The 'Ball-and-stick model' image provides a three-dimensional representation of Prenol, illustrating how the atoms are connected and their relative positions in space, which helps in understanding the molecule's shape.
  • What does the image labeled 'Skeletal formula of prenol' depict?: The image labeled 'Skeletal formula of prenol' displays a simplified representation of the Prenol molecule's chemical structure, showing the arrangement of carbon and oxygen atoms and their bonds without explicitly drawing all hydrogen atoms.

What is the preferred IUPAC name for Prenol?

Answer: 3-Methylbut-2-en-1-ol

The preferred IUPAC name for Prenol, established by systematic nomenclature, is 3-Methylbut-2-en-1-ol. This designation ensures clarity and consistency in chemical identification.

Related Concepts:

  • What is the preferred IUPAC nomenclature for Prenol?: The preferred IUPAC nomenclature for Prenol is 3-Methylbut-2-en-1-ol. Adherence to IUPAC nomenclature ensures systematic and unambiguous identification of chemical compounds within the scientific community.
  • What are some common names used for Prenol?: Besides its preferred IUPAC name, Prenol is also commonly known as 3,3-Dimethylallyl alcohol. These alternative names are frequently encountered in scientific literature and industrial contexts.
  • What is Prenol's identifier on the ChemSpider database?: Prenol is identified by the number 10700 on ChemSpider, a comprehensive chemical database that provides access to information regarding chemical structures and properties.

Which of the following is NOT a common name or identifier for Prenol listed in the source?

Answer: Prenal

Prenal is an aldehyde derived from Prenol via oxidation. It is not a common name or identifier for Prenol itself. The other options are valid identifiers or common names for Prenol.

Related Concepts:

  • What is the PubChem Compound ID (CID) for Prenol?: The PubChem Compound ID for Prenol is 11173. PubChem is a widely used database for chemical molecules and their associated activities, and this CID allows for precise retrieval of Prenol's data.
  • What is the ChEBI identifier for Prenol?: The ChEBI (Chemical Entities of Biological Interest) identifier for Prenol is CHEBI:16019. This designation is utilized in biological and chemical databases for referencing the compound.
  • What is Prenol's identifier on the ChemSpider database?: Prenol is identified by the number 10700 on ChemSpider, a comprehensive chemical database that provides access to information regarding chemical structures and properties.

What is the chemical formula for Prenol?

Answer: C5H10O

The chemical formula for Prenol is C5H10O, indicating a molecular structure composed of five carbon atoms, ten hydrogen atoms, and one oxygen atom.

Related Concepts:

  • What is Prenol's identifier on the ChemSpider database?: Prenol is identified by the number 10700 on ChemSpider, a comprehensive chemical database that provides access to information regarding chemical structures and properties.
  • What is the chemical formula for Prenol?: The chemical formula for Prenol is C5H10O. This formula indicates that each molecule of Prenol comprises 5 carbon atoms, 10 hydrogen atoms, and 1 oxygen atom.
  • What is the PubChem Compound ID (CID) for Prenol?: The PubChem Compound ID for Prenol is 11173. PubChem is a widely used database for chemical molecules and their associated activities, and this CID allows for precise retrieval of Prenol's data.

Prenol has a molar mass of approximately:

Answer: 86.132 g/mol

The precise molar mass of Prenol is calculated to be 86.132 g/mol, a fundamental property used in stoichiometric calculations.

Related Concepts:

  • What is the molar mass of Prenol?: The molar mass of Prenol is 86.132 g/mol. This fundamental property is essential for quantitative chemical analysis and calculations.
  • What was the estimated global production volume of Prenol in 2001?: In 2001, the global production of Prenol was estimated to be between 6,000 and 13,000 tons. This indicates a significant industrial scale of production.
  • What is Prenol's identifier on the ChemSpider database?: Prenol is identified by the number 10700 on ChemSpider, a comprehensive chemical database that provides access to information regarding chemical structures and properties.

Which identifier is assigned to Prenol by the PubChem database?

Answer: 11173

The PubChem database assigns the Compound ID (CID) 11173 to Prenol, facilitating its retrieval and study within that comprehensive chemical information resource.

Related Concepts:

  • What is the PubChem Compound ID (CID) for Prenol?: The PubChem Compound ID for Prenol is 11173. PubChem is a widely used database for chemical molecules and their associated activities, and this CID allows for precise retrieval of Prenol's data.
  • What is the ChEBI identifier for Prenol?: The ChEBI (Chemical Entities of Biological Interest) identifier for Prenol is CHEBI:16019. This designation is utilized in biological and chemical databases for referencing the compound.
  • What is Prenol's identifier on the ChemSpider database?: Prenol is identified by the number 10700 on ChemSpider, a comprehensive chemical database that provides access to information regarding chemical structures and properties.

The source mentions an interactive 3D model of Prenol is available via which platform?

Answer: JSmol

An interactive 3D model for visualizing Prenol's molecular structure is accessible through the JSmol platform, as indicated in the provided information.

Related Concepts:

  • Where can one access an interactive 3D model of Prenol?: An interactive 3D model of Prenol is accessible through the JSmol platform, providing a dynamic visualization of its molecular structure.
  • What information is conveyed by the 'Ball-and-stick model' image of Prenol?: The 'Ball-and-stick model' image provides a three-dimensional representation of Prenol, illustrating how the atoms are connected and their relative positions in space, which helps in understanding the molecule's shape.

The ECHA InfoCard number for Prenol is:

Answer: 100.008.312

The ECHA InfoCard number assigned to Prenol is 100.008.312, providing regulatory information within the European Chemicals Agency framework.

Related Concepts:

  • What is the ECHA InfoCard number for Prenol?: The ECHA (European Chemicals Agency) InfoCard number for Prenol is 100.008.312. This identifier serves as a gateway to regulatory information pertaining to the substance within the European Union.
  • What is Prenol's EC Number?: Prenol possesses an EC Number of 209-141-4. This number is assigned by the European Commission to uniquely identify chemical substances within the European market.
  • What is Prenol's identifier on the ChemSpider database?: Prenol is identified by the number 10700 on ChemSpider, a comprehensive chemical database that provides access to information regarding chemical structures and properties.

The standard InChI representation for Prenol includes a specific key. What is this key?

Answer: ASUAYTHWZCLXAN-UHFFFAOYSA-N

The standard InChI key for Prenol is ASUAYTHWZCLXAN-UHFFFAOYSA-N, which serves as a unique, canonical textual identifier for its chemical structure.

Related Concepts:

  • What is the standard InChI representation of Prenol?: The standard InChI (International Chemical Identifier) for Prenol is InChI=1S/C5H10O/c1-5(2)3-4-6/h3,6H,4H2,1-2H3, with the corresponding key being ASUAYTHWZCLXAN-UHFFFAOYSA-N. InChI provides a canonical textual representation of chemical structures.
  • What is the ChEBI identifier for Prenol?: The ChEBI (Chemical Entities of Biological Interest) identifier for Prenol is CHEBI:16019. This designation is utilized in biological and chemical databases for referencing the compound.
  • What is Prenol's identifier on the ChemSpider database?: Prenol is identified by the number 10700 on ChemSpider, a comprehensive chemical database that provides access to information regarding chemical structures and properties.

Physical Properties

Prenol is a solid at room temperature, with a melting point above 0°C.

Answer: False

Prenol is a clear, colorless oil at room temperature, not a solid. Its melting point is approximately -59°C, well below 0°C.

Related Concepts:

  • What is the melting point of Prenol?: The melting point of Prenol is calculated to be -59 °C (-74 °F; 214 K). This is the temperature at which Prenol transitions from a solid to a liquid state under standard pressure.
  • What is the flash point of Prenol?: The flash point of Prenol is 43.3 °C (109.9 °F; 316.4 K). The flash point is the lowest temperature at which a liquid can form an ignitable mixture in air near its surface.
  • What is the boiling point of Prenol?: The boiling point of Prenol is approximately 142 °C (288 °F; 415 K). This is the temperature at which Prenol vaporizes under standard pressure.

Prenol is highly soluble in water, dissolving completely at 20°C.

Answer: False

Prenol exhibits moderate solubility in water, with a value of 17 grams per 100 milliliters at 20°C. It does not dissolve completely.

Related Concepts:

  • How soluble is Prenol in water?: Prenol exhibits a solubility of 17 grams per 100 milliliters in water at 20 °C. This indicates moderate solubility, meaning a significant amount can dissolve.
  • What is Prenol's identifier on the ChemSpider database?: Prenol is identified by the number 10700 on ChemSpider, a comprehensive chemical database that provides access to information regarding chemical structures and properties.
  • What is the partition coefficient (log P) for Prenol?: Prenol has a log P value of 0.91. The partition coefficient measures a chemical's relative solubility in octanol versus water, offering insight into its lipophilicity and behavior in biological systems.

Prenol's flash point is above the boiling point of water.

Answer: False

Prenol's flash point is approximately 43.3°C, whereas the boiling point of water is 100°C. Therefore, Prenol's flash point is below the boiling point of water.

Related Concepts:

  • What is the flash point of Prenol?: The flash point of Prenol is 43.3 °C (109.9 °F; 316.4 K). The flash point is the lowest temperature at which a liquid can form an ignitable mixture in air near its surface.
  • How does the flash point of Prenol relate to its safety classification?: While there might be slight variations in reported flash points (e.g., 43.3 °C vs. 51.5 °C), the value consistently classifies Prenol as a flammable liquid. For instance, it falls under GHS category 3 for flammable liquids, indicating it requires careful handling to prevent fire hazards.
  • What is the boiling point of Prenol?: The boiling point of Prenol is approximately 142 °C (288 °F; 415 K). This is the temperature at which Prenol vaporizes under standard pressure.

Prenol's density is less than that of water.

Answer: True

Prenol has a density of approximately 0.848 g/cm³, which is less than the density of water (approximately 1 g/cm³).

Related Concepts:

  • What is the density of Prenol?: Prenol has a density of 0.848 g/cm³. Density quantifies mass per unit volume, providing insight into the substance's compactness.
  • How soluble is Prenol in water?: Prenol exhibits a solubility of 17 grams per 100 milliliters in water at 20 °C. This indicates moderate solubility, meaning a significant amount can dissolve.
  • What is Prenol's identifier on the ChemSpider database?: Prenol is identified by the number 10700 on ChemSpider, a comprehensive chemical database that provides access to information regarding chemical structures and properties.

Prenol is described as having a pungent, chemical odor.

Answer: False

Prenol is described as having a fruity odor, which makes it suitable for use in perfumery. A pungent, chemical odor is not its characteristic scent.

Related Concepts:

  • Describe the physical appearance and odor of Prenol.: Prenol is described as a clear, colorless oil. It possesses a fruity odor, which makes it suitable for occasional use in perfumery.
  • What is the GHS signal word for Prenol?: The GHS signal word for Prenol is 'Warning'. This designation indicates a less severe level of hazard compared to the signal word 'Danger'.
  • What is Prenol's identifier on the ChemSpider database?: Prenol is identified by the number 10700 on ChemSpider, a comprehensive chemical database that provides access to information regarding chemical structures and properties.

The vapor pressure of Prenol at 25°C is significantly higher than 100 hPa.

Answer: False

The vapor pressure of Prenol at 25°C is approximately 3.17 hPa, which is substantially lower than 100 hPa.

Related Concepts:

  • What is the vapor pressure of Prenol at 25 °C?: The vapor pressure of Prenol at 25 °C is extrapolated to be 3.17 hPa. Vapor pressure quantifies a substance's tendency to transition into the gaseous state.
  • What is the boiling point of Prenol?: The boiling point of Prenol is approximately 142 °C (288 °F; 415 K). This is the temperature at which Prenol vaporizes under standard pressure.
  • How does the flash point of Prenol relate to its safety classification?: While there might be slight variations in reported flash points (e.g., 43.3 °C vs. 51.5 °C), the value consistently classifies Prenol as a flammable liquid. For instance, it falls under GHS category 3 for flammable liquids, indicating it requires careful handling to prevent fire hazards.

Prenol's log P value of 0.91 suggests it is highly lipophilic.

Answer: False

A log P value of 0.91 indicates moderate solubility in both aqueous and lipid-like environments, rather than high lipophilicity. Highly lipophilic compounds typically have much higher log P values.

Related Concepts:

  • What is the partition coefficient (log P) for Prenol?: Prenol has a log P value of 0.91. The partition coefficient measures a chemical's relative solubility in octanol versus water, offering insight into its lipophilicity and behavior in biological systems.
  • How soluble is Prenol in water?: Prenol exhibits a solubility of 17 grams per 100 milliliters in water at 20 °C. This indicates moderate solubility, meaning a significant amount can dissolve.
  • What is Prenol's identifier on the ChemSpider database?: Prenol is identified by the number 10700 on ChemSpider, a comprehensive chemical database that provides access to information regarding chemical structures and properties.

What is the approximate boiling point of Prenol?

Answer: 142 °C

Prenol exhibits a boiling point of approximately 142°C at standard atmospheric pressure, indicating its volatility characteristics.

Related Concepts:

  • What is the boiling point of Prenol?: The boiling point of Prenol is approximately 142 °C (288 °F; 415 K). This is the temperature at which Prenol vaporizes under standard pressure.
  • What is the flash point of Prenol?: The flash point of Prenol is 43.3 °C (109.9 °F; 316.4 K). The flash point is the lowest temperature at which a liquid can form an ignitable mixture in air near its surface.
  • What is the melting point of Prenol?: The melting point of Prenol is calculated to be -59 °C (-74 °F; 214 K). This is the temperature at which Prenol transitions from a solid to a liquid state under standard pressure.

Prenol is described as having which physical characteristics?

Answer: A clear, colorless oil with a fruity odor

Prenol is characterized as a clear, colorless oil possessing a distinct fruity odor, which contributes to its use in perfumery.

Related Concepts:

  • What is the density of Prenol?: Prenol has a density of 0.848 g/cm³. Density quantifies mass per unit volume, providing insight into the substance's compactness.
  • Describe the physical appearance and odor of Prenol.: Prenol is described as a clear, colorless oil. It possesses a fruity odor, which makes it suitable for occasional use in perfumery.
  • What is Prenol's identifier on the ChemSpider database?: Prenol is identified by the number 10700 on ChemSpider, a comprehensive chemical database that provides access to information regarding chemical structures and properties.

What does the partition coefficient (log P) of 0.91 for Prenol indicate?

Answer: Prenol has moderate solubility in both water and lipid-like environments.

A log P value of 0.91 suggests that Prenol exhibits balanced solubility, indicating it partitions moderately between aqueous and lipid phases. This is neither extremely high nor low lipophilicity.

Related Concepts:

  • What is the partition coefficient (log P) for Prenol?: Prenol has a log P value of 0.91. The partition coefficient measures a chemical's relative solubility in octanol versus water, offering insight into its lipophilicity and behavior in biological systems.
  • How soluble is Prenol in water?: Prenol exhibits a solubility of 17 grams per 100 milliliters in water at 20 °C. This indicates moderate solubility, meaning a significant amount can dissolve.

What is the density of Prenol?

Answer: 0.848 g/cm³

The density of Prenol is reported as 0.848 g/cm³, a value crucial for various physical and chemical calculations.

Related Concepts:

  • What is the density of Prenol?: Prenol has a density of 0.848 g/cm³. Density quantifies mass per unit volume, providing insight into the substance's compactness.
  • What is the molar mass of Prenol?: The molar mass of Prenol is 86.132 g/mol. This fundamental property is essential for quantitative chemical analysis and calculations.
  • What is Prenol's identifier on the ChemSpider database?: Prenol is identified by the number 10700 on ChemSpider, a comprehensive chemical database that provides access to information regarding chemical structures and properties.

What is the flash point of Prenol?

Answer: 43.3 °C

The flash point of Prenol is approximately 43.3°C (109.9°F). This value is critical for assessing its flammability hazards.

Related Concepts:

  • What is the flash point of Prenol?: The flash point of Prenol is 43.3 °C (109.9 °F; 316.4 K). The flash point is the lowest temperature at which a liquid can form an ignitable mixture in air near its surface.
  • How does the flash point of Prenol relate to its safety classification?: While there might be slight variations in reported flash points (e.g., 43.3 °C vs. 51.5 °C), the value consistently classifies Prenol as a flammable liquid. For instance, it falls under GHS category 3 for flammable liquids, indicating it requires careful handling to prevent fire hazards.
  • What is the boiling point of Prenol?: The boiling point of Prenol is approximately 142 °C (288 °F; 415 K). This is the temperature at which Prenol vaporizes under standard pressure.

Safety and Hazard Classification

The GHS pictograms for Prenol indicate it is non-flammable and non-toxic.

Answer: False

GHS pictograms for Prenol include a flame (indicating flammability) and an exclamation mark (indicating it is harmful if swallowed). It is not classified as non-flammable or non-toxic.

Related Concepts:

  • What GHS pictograms are associated with Prenol?: Prenol is associated with two GHS pictograms: a flame, indicating it is a flammable liquid, and an exclamation mark, signifying it is harmful if swallowed (acute toxicity category 4). These pictograms are standardized symbols for hazard communication.
  • What are some key GHS precautionary statements for handling Prenol?: Key GHS precautionary statements for Prenol include P210 (Keep away from heat, sparks, open flames), P233 (Keep container tightly closed), P264 (Wash thoroughly after handling), and P270 (Do not eat, drink or smoke when using this product). These guide safe handling and storage practices.
  • What is the GHS signal word for Prenol?: The GHS signal word for Prenol is 'Warning'. This designation indicates a less severe level of hazard compared to the signal word 'Danger'.

The GHS signal word for Prenol is 'Danger'.

Answer: False

The Globally Harmonized System (GHS) signal word assigned to Prenol is 'Warning', indicating a lower severity of hazard compared to 'Danger'.

Related Concepts:

  • What is the GHS signal word for Prenol?: The GHS signal word for Prenol is 'Warning'. This designation indicates a less severe level of hazard compared to the signal word 'Danger'.
  • What GHS pictograms are associated with Prenol?: Prenol is associated with two GHS pictograms: a flame, indicating it is a flammable liquid, and an exclamation mark, signifying it is harmful if swallowed (acute toxicity category 4). These pictograms are standardized symbols for hazard communication.
  • What are the GHS hazard statements for Prenol?: The GHS hazard statements for Prenol include H226 ('Flammable liquid and vapor') and H302 ('Harmful if swallowed'). These statements provide specific details regarding the risks associated with the chemical.

Prenol is classified under GHS hazard statement H315, meaning 'Causes skin irritation'.

Answer: False

The primary GHS hazard statements for Prenol are H226 ('Flammable liquid and vapor') and H302 ('Harmful if swallowed'). H315 ('Causes skin irritation') is not listed as a primary hazard.

Related Concepts:

  • What are some key GHS precautionary statements for handling Prenol?: Key GHS precautionary statements for Prenol include P210 (Keep away from heat, sparks, open flames), P233 (Keep container tightly closed), P264 (Wash thoroughly after handling), and P270 (Do not eat, drink or smoke when using this product). These guide safe handling and storage practices.
  • What are the GHS hazard statements for Prenol?: The GHS hazard statements for Prenol include H226 ('Flammable liquid and vapor') and H302 ('Harmful if swallowed'). These statements provide specific details regarding the risks associated with the chemical.
  • What is the GHS signal word for Prenol?: The GHS signal word for Prenol is 'Warning'. This designation indicates a less severe level of hazard compared to the signal word 'Danger'.

According to the GHS classification, Prenol is considered:

Answer: A flammable liquid and harmful if swallowed

The GHS classification for Prenol includes hazard statements indicating it is a flammable liquid (H226) and harmful if swallowed (H302).

Related Concepts:

  • What is the GHS signal word for Prenol?: The GHS signal word for Prenol is 'Warning'. This designation indicates a less severe level of hazard compared to the signal word 'Danger'.
  • What are the GHS hazard statements for Prenol?: The GHS hazard statements for Prenol include H226 ('Flammable liquid and vapor') and H302 ('Harmful if swallowed'). These statements provide specific details regarding the risks associated with the chemical.
  • What are some key GHS precautionary statements for handling Prenol?: Key GHS precautionary statements for Prenol include P210 (Keep away from heat, sparks, open flames), P233 (Keep container tightly closed), P264 (Wash thoroughly after handling), and P270 (Do not eat, drink or smoke when using this product). These guide safe handling and storage practices.

Which GHS pictogram is associated with Prenol due to its flammability?

Answer: Flame

The GHS pictogram depicting a flame is associated with Prenol, signifying its classification as a flammable liquid and vapor.

Related Concepts:

  • What GHS pictograms are associated with Prenol?: Prenol is associated with two GHS pictograms: a flame, indicating it is a flammable liquid, and an exclamation mark, signifying it is harmful if swallowed (acute toxicity category 4). These pictograms are standardized symbols for hazard communication.
  • What is the GHS signal word for Prenol?: The GHS signal word for Prenol is 'Warning'. This designation indicates a less severe level of hazard compared to the signal word 'Danger'.
  • What are the GHS hazard statements for Prenol?: The GHS hazard statements for Prenol include H226 ('Flammable liquid and vapor') and H302 ('Harmful if swallowed'). These statements provide specific details regarding the risks associated with the chemical.

What hazard is indicated by the GHS hazard statement H302 for Prenol?

Answer: Harmful if swallowed

The GHS hazard statement H302 specifically denotes that the substance is 'Harmful if swallowed', representing an acute toxicity risk.

Related Concepts:

  • What are the GHS hazard statements for Prenol?: The GHS hazard statements for Prenol include H226 ('Flammable liquid and vapor') and H302 ('Harmful if swallowed'). These statements provide specific details regarding the risks associated with the chemical.
  • What are some key GHS precautionary statements for handling Prenol?: Key GHS precautionary statements for Prenol include P210 (Keep away from heat, sparks, open flames), P233 (Keep container tightly closed), P264 (Wash thoroughly after handling), and P270 (Do not eat, drink or smoke when using this product). These guide safe handling and storage practices.
  • What is the GHS signal word for Prenol?: The GHS signal word for Prenol is 'Warning'. This designation indicates a less severe level of hazard compared to the signal word 'Danger'.

Which of the following is a key precautionary statement for handling Prenol?

Answer: Keep away from heat, sparks, and open flames.

Given Prenol's classification as a flammable liquid (H226), a critical precautionary statement (P210) is to keep it away from heat, sparks, and open flames to prevent ignition.

Related Concepts:

  • What are some key GHS precautionary statements for handling Prenol?: Key GHS precautionary statements for Prenol include P210 (Keep away from heat, sparks, open flames), P233 (Keep container tightly closed), P264 (Wash thoroughly after handling), and P270 (Do not eat, drink or smoke when using this product). These guide safe handling and storage practices.
  • What are the GHS hazard statements for Prenol?: The GHS hazard statements for Prenol include H226 ('Flammable liquid and vapor') and H302 ('Harmful if swallowed'). These statements provide specific details regarding the risks associated with the chemical.
  • What is the GHS signal word for Prenol?: The GHS signal word for Prenol is 'Warning'. This designation indicates a less severe level of hazard compared to the signal word 'Danger'.

What is the GHS signal word assigned to Prenol?

Answer: Warning

The Globally Harmonized System (GHS) assigns the signal word 'Warning' to Prenol, indicating a moderate level of hazard.

Related Concepts:

  • What is the GHS signal word for Prenol?: The GHS signal word for Prenol is 'Warning'. This designation indicates a less severe level of hazard compared to the signal word 'Danger'.
  • What GHS pictograms are associated with Prenol?: Prenol is associated with two GHS pictograms: a flame, indicating it is a flammable liquid, and an exclamation mark, signifying it is harmful if swallowed (acute toxicity category 4). These pictograms are standardized symbols for hazard communication.
  • What are the GHS hazard statements for Prenol?: The GHS hazard statements for Prenol include H226 ('Flammable liquid and vapor') and H302 ('Harmful if swallowed'). These statements provide specific details regarding the risks associated with the chemical.

Industrial Production and Applications

Prenol is primarily used as a solvent in industrial cleaning applications.

Answer: False

The primary industrial application of Prenol is as a precursor for the synthesis of citral, which is subsequently used in the production of vitamins A, E, and K. It is not primarily used as a solvent for cleaning.

Related Concepts:

  • Which companies are known to manufacture Prenol industrially?: Prenol is manufactured industrially by companies such as BASF in Germany and Kuraray in Asia. These companies produce it as an intermediate for pharmaceuticals and aroma compounds.
  • What are some key GHS precautionary statements for handling Prenol?: Key GHS precautionary statements for Prenol include P210 (Keep away from heat, sparks, open flames), P233 (Keep container tightly closed), P264 (Wash thoroughly after handling), and P270 (Do not eat, drink or smoke when using this product). These guide safe handling and storage practices.
  • How does the flash point of Prenol relate to its safety classification?: While there might be slight variations in reported flash points (e.g., 43.3 °C vs. 51.5 °C), the value consistently classifies Prenol as a flammable liquid. For instance, it falls under GHS category 3 for flammable liquids, indicating it requires careful handling to prevent fire hazards.

The industrial production of Prenol involves the isomerization of isoprenol.

Answer: True

Industrial synthesis of Prenol typically involves the initial formation of isoprenol (3-methyl-3-buten-1-ol) from isobutene and formaldehyde, followed by the isomerization of isoprenol to yield Prenol (3-methyl-2-buten-1-ol).

Related Concepts:

  • What is the role of isoprenol in Prenol's industrial production?: Isoprenol, specifically 3-methyl-3-buten-1-ol, is an intermediate product in the industrial synthesis of Prenol. It is formed first from the reaction of isobutene and formaldehyde, and then isomerized into Prenol.
  • What chemical transformation is shown in the image titled 'The isomerization of isoprenol to prenol'?: The image titled 'The isomerization of isoprenol to prenol' depicts the second step in the industrial synthesis of Prenol, illustrating the chemical rearrangement of isoprenol into Prenol.
  • What is the industrial process for producing Prenol?: Industrially, Prenol is produced by reacting formaldehyde with isobutene to form isoprenol (3-methyl-3-buten-1-ol), which is then isomerized to yield Prenol (3-methyl-2-buten-1-ol).

Prenol is manufactured industrially by companies located exclusively in Germany.

Answer: False

Industrial production of Prenol occurs in multiple regions, including Germany (e.g., by BASF) and Asia (e.g., by Kuraray), not exclusively in Germany.

Related Concepts:

  • Which companies are known to manufacture Prenol industrially?: Prenol is manufactured industrially by companies such as BASF in Germany and Kuraray in Asia. These companies produce it as an intermediate for pharmaceuticals and aroma compounds.
  • What was the estimated global production volume of Prenol in 2001?: In 2001, the global production of Prenol was estimated to be between 6,000 and 13,000 tons. This indicates a significant industrial scale of production.
  • What is the industrial process for producing Prenol?: Industrially, Prenol is produced by reacting formaldehyde with isobutene to form isoprenol (3-methyl-3-buten-1-ol), which is then isomerized to yield Prenol (3-methyl-2-buten-1-ol).

Prenol is used as an intermediate in the synthesis of Vitamin C.

Answer: False

Prenol serves as an intermediate in the synthesis of citral, which is then used for producing vitamins A, E, and K. It is not directly involved in Vitamin C synthesis.

Related Concepts:

  • What is the primary use of Prenol in industrial applications?: Prenol is primarily used as a precursor for the industrial production of citral. Citral, in turn, is an important intermediate in the synthesis of vitamins A, E, and K.
  • What aldehyde is produced when Prenol is oxidized?: When Prenol is oxidized, it produces the aldehyde known as prenal. This aldehyde is a key step in the pathway to synthesizing citral.
  • Which companies are known to manufacture Prenol industrially?: Prenol is manufactured industrially by companies such as BASF in Germany and Kuraray in Asia. These companies produce it as an intermediate for pharmaceuticals and aroma compounds.

Isoprenol is the final product in the industrial synthesis of Prenol.

Answer: False

Isoprenol (3-methyl-3-buten-1-ol) is an intermediate compound in the industrial production of Prenol (3-methyl-2-buten-1-ol). Prenol is the final product of this specific synthetic step.

Related Concepts:

  • What is the role of isoprenol in Prenol's industrial production?: Isoprenol, specifically 3-methyl-3-buten-1-ol, is an intermediate product in the industrial synthesis of Prenol. It is formed first from the reaction of isobutene and formaldehyde, and then isomerized into Prenol.
  • What is the industrial process for producing Prenol?: Industrially, Prenol is produced by reacting formaldehyde with isobutene to form isoprenol (3-methyl-3-buten-1-ol), which is then isomerized to yield Prenol (3-methyl-2-buten-1-ol).
  • What chemical transformation is shown in the image titled 'The isomerization of isoprenol to prenol'?: The image titled 'The isomerization of isoprenol to prenol' depicts the second step in the industrial synthesis of Prenol, illustrating the chemical rearrangement of isoprenol into Prenol.

What is the primary industrial application of Prenol mentioned in the source?

Answer: Precursor for citral synthesis (leading to vitamins A, E, K)

Prenol serves as a crucial intermediate in the industrial synthesis of citral, which is subsequently utilized in the production of essential vitamins such as A, E, and K.

Related Concepts:

  • Which companies are known to manufacture Prenol industrially?: Prenol is manufactured industrially by companies such as BASF in Germany and Kuraray in Asia. These companies produce it as an intermediate for pharmaceuticals and aroma compounds.
  • What is the industrial process for producing Prenol?: Industrially, Prenol is produced by reacting formaldehyde with isobutene to form isoprenol (3-methyl-3-buten-1-ol), which is then isomerized to yield Prenol (3-methyl-2-buten-1-ol).
  • What is the primary use of Prenol in industrial applications?: Prenol is primarily used as a precursor for the industrial production of citral. Citral, in turn, is an important intermediate in the synthesis of vitamins A, E, and K.

Which of the following is an isomer of Prenol involved in its industrial production?

Answer: Isoprenol (3-methyl-3-buten-1-ol)

Isoprenol, specifically 3-methyl-3-buten-1-ol, is an isomer of Prenol and serves as a key intermediate in its industrial synthesis pathway.

Related Concepts:

  • What is the industrial process for producing Prenol?: Industrially, Prenol is produced by reacting formaldehyde with isobutene to form isoprenol (3-methyl-3-buten-1-ol), which is then isomerized to yield Prenol (3-methyl-2-buten-1-ol).
  • Which companies are known to manufacture Prenol industrially?: Prenol is manufactured industrially by companies such as BASF in Germany and Kuraray in Asia. These companies produce it as an intermediate for pharmaceuticals and aroma compounds.
  • What is the role of isoprenol in Prenol's industrial production?: Isoprenol, specifically 3-methyl-3-buten-1-ol, is an intermediate product in the industrial synthesis of Prenol. It is formed first from the reaction of isobutene and formaldehyde, and then isomerized into Prenol.

What was the estimated global production volume of Prenol in 2001?

Answer: 6,000-13,000 tons

In the year 2001, the estimated global production volume for Prenol ranged between 6,000 and 13,000 tons, indicating a substantial industrial output.

Related Concepts:

  • What was the estimated global production volume of Prenol in 2001?: In 2001, the global production of Prenol was estimated to be between 6,000 and 13,000 tons. This indicates a significant industrial scale of production.
  • Which companies are known to manufacture Prenol industrially?: Prenol is manufactured industrially by companies such as BASF in Germany and Kuraray in Asia. These companies produce it as an intermediate for pharmaceuticals and aroma compounds.
  • What is Prenol's identifier on the ChemSpider database?: Prenol is identified by the number 10700 on ChemSpider, a comprehensive chemical database that provides access to information regarding chemical structures and properties.

Which company manufactures Prenol in Asia, according to the provided text?

Answer: Kuraray

The text specifies that Kuraray is one of the companies known for the industrial manufacture of Prenol, with operations located in Asia.

Related Concepts:

  • Which companies are known to manufacture Prenol industrially?: Prenol is manufactured industrially by companies such as BASF in Germany and Kuraray in Asia. These companies produce it as an intermediate for pharmaceuticals and aroma compounds.

Natural Occurrence and Biological Context

Prenol is exclusively found in synthetic chemical processes and does not occur naturally.

Answer: False

Prenol occurs naturally in various fruits and plants, such as citrus fruits, berries, tomato, and coffee, in addition to being produced synthetically.

Related Concepts:

  • What is the industrial process for producing Prenol?: Industrially, Prenol is produced by reacting formaldehyde with isobutene to form isoprenol (3-methyl-3-buten-1-ol), which is then isomerized to yield Prenol (3-methyl-2-buten-1-ol).
  • Which companies are known to manufacture Prenol industrially?: Prenol is manufactured industrially by companies such as BASF in Germany and Kuraray in Asia. These companies produce it as an intermediate for pharmaceuticals and aroma compounds.
  • What is Prenol, and where does it occur naturally?: Prenol, also known as 3-methyl-2-buten-1-ol, is a natural alcohol and one of the simplest terpenoids. It is found naturally in various fruits (e.g., citrus, berries) and plants (e.g., tomato, coffee).

Prenol is classified as a terpenoid, specifically one of the simplest examples.

Answer: True

Prenol is indeed classified as a terpenoid, representing one of the most fundamental structures within this class of organic compounds derived from isoprene units.

Related Concepts:

  • What is Prenol, and where does it occur naturally?: Prenol, also known as 3-methyl-2-buten-1-ol, is a natural alcohol and one of the simplest terpenoids. It is found naturally in various fruits (e.g., citrus, berries) and plants (e.g., tomato, coffee).
  • How does Prenol relate to the concept of 'isoprenols'?: Prenol is considered one of the simplest terpenoids and is a building block for isoprenoid alcohols, which are sometimes referred to as 'isoprenols' due to their structural relation to isoprene units. However, it is important not to confuse Prenol with its isomer, isoprenol (3-methyl-3-buten-1-ol).
  • Describe the physical appearance and odor of Prenol.: Prenol is described as a clear, colorless oil. It possesses a fruity odor, which makes it suitable for occasional use in perfumery.

Dolichols are unsaturated isoprenoid alcohols similar in structure to Prenol.

Answer: False

Dolichols are isoprenoid alcohols, but they are characterized by a saturated isoprene unit attached to the alcohol group, distinguishing them from unsaturated compounds like Prenol.

Related Concepts:

  • What are dolichols, and how do they differ from isoprenoid alcohols like Prenol?: Dolichols are isoprenoid alcohols where the isoprene unit attached to the alcohol group is saturated (meaning it contains no double bonds). They are distinct from unsaturated isoprenoid alcohols like Prenol and its derivatives.
  • What is the biological significance of dolichols?: Dolichols play crucial roles in biological processes, serving as glycosyl carriers in the synthesis of polysaccharides. They also help protect cellular membranes, stabilize cell proteins, and support the immune system.
  • What is the significance of ingested polyprenols for human and animal health?: Ingested polyprenols are metabolized by the liver into dolichols, which can then participate in the dolichol phosphate cycle and be assimilated by the body. This process is thought to be beneficial, particularly in cases of dolichol deficits associated with inflammatory, degenerative, or oncological diseases.

Polyprenols are short-chain alcohols containing only 2 or 3 isoprene units.

Answer: False

Polyprenols are defined as long-chain isoprenoid alcohols containing a minimum of five isoprene units (n ≥ 5), and can extend up to 100 units. Short-chain variants are typically referred to by other names.

Related Concepts:

  • How are polyprenols formed, and what is their general structure?: Polyprenols are formed through dehydration reactions involving prenol, resulting in polymers with at least five isoprene units (n ≥ 5 in the general formula H–[CH₂CCH₃=CHCH₂]n–OH). These long-chain alcohols, also called 'terpenols', retain a hydroxyl group at one end and can contain up to 100 isoprene units.
  • What are isoprenoid alcohols, and what is their general formula?: Isoprenoid alcohols are compounds built from repeating isoprene units. Their general formula is H–[CH₂CCH₃=CHCH₂]n–OH, where the repeating C₅H₈ unit is derived from isoprene. Prenol itself is the simplest example of such a structure.
  • What roles do polyprenols and related long-chain isoprenoid alcohols play in biological systems?: These long-chain isoprenoid alcohols, including polyprenols, are important in the acylation of proteins, carotenoids, and fat-soluble vitamins such as A, E, and K. They are also involved in cell metabolism.

Live conifer needles are a poor source for extracting polyprenols.

Answer: False

Live conifer needles are identified as one of the richest and most widely available natural sources for the extraction of polyprenols.

Related Concepts:

  • What is a readily available natural source for extracting polyprenols?: Live conifer needles are identified as one of the richest and most widely available natural sources for extracting polyprenols. Commercial extraction methods are designed to preserve the biological activity of these compounds.

What is the significance of dolichols, which are related to Prenol?

Answer: They act as glycosyl carriers in polysaccharide synthesis and protect cell membranes.

Dolichols play vital biological roles, including functioning as glycosyl carriers essential for polysaccharide synthesis and contributing to the protection and stabilization of cellular membranes.

Related Concepts:

  • What are dolichols, and how do they differ from isoprenoid alcohols like Prenol?: Dolichols are isoprenoid alcohols where the isoprene unit attached to the alcohol group is saturated (meaning it contains no double bonds). They are distinct from unsaturated isoprenoid alcohols like Prenol and its derivatives.
  • What is the significance of ingested polyprenols for human and animal health?: Ingested polyprenols are metabolized by the liver into dolichols, which can then participate in the dolichol phosphate cycle and be assimilated by the body. This process is thought to be beneficial, particularly in cases of dolichol deficits associated with inflammatory, degenerative, or oncological diseases.
  • What is the biological significance of dolichols?: Dolichols play crucial roles in biological processes, serving as glycosyl carriers in the synthesis of polysaccharides. They also help protect cellular membranes, stabilize cell proteins, and support the immune system.

Prenol is structurally related to which class of compounds, often built from repeating isoprene units?

Answer: Isoprenoid alcohols

Prenol is classified as an isoprenoid alcohol, a class of organic compounds characterized by structures derived from repeating isoprene units.

Related Concepts:

  • What are isoprenoid alcohols, and what is their general formula?: Isoprenoid alcohols are compounds built from repeating isoprene units. Their general formula is H–[CH₂CCH₃=CHCH₂]n–OH, where the repeating C₅H₈ unit is derived from isoprene. Prenol itself is the simplest example of such a structure.
  • How does Prenol relate to the concept of 'isoprenols'?: Prenol is considered one of the simplest terpenoids and is a building block for isoprenoid alcohols, which are sometimes referred to as 'isoprenols' due to their structural relation to isoprene units. However, it is important not to confuse Prenol with its isomer, isoprenol (3-methyl-3-buten-1-ol).
  • How are polyprenols formed, and what is their general structure?: Polyprenols are formed through dehydration reactions involving prenol, resulting in polymers with at least five isoprene units (n ≥ 5 in the general formula H–[CH₂CCH₃=CHCH₂]n–OH). These long-chain alcohols, also called 'terpenols', retain a hydroxyl group at one end and can contain up to 100 isoprene units.

What is the primary role of polyprenols in biological systems, according to the source?

Answer: Protein acylation and synthesis of fat-soluble vitamins

Polyprenols and related long-chain isoprenoid alcohols are significant in biological systems for their roles in protein acylation and the synthesis of fat-soluble vitamins, including A, E, and K.

Related Concepts:

  • What is the significance of ingested polyprenols for human and animal health?: Ingested polyprenols are metabolized by the liver into dolichols, which can then participate in the dolichol phosphate cycle and be assimilated by the body. This process is thought to be beneficial, particularly in cases of dolichol deficits associated with inflammatory, degenerative, or oncological diseases.
  • What roles do polyprenols and related long-chain isoprenoid alcohols play in biological systems?: These long-chain isoprenoid alcohols, including polyprenols, are important in the acylation of proteins, carotenoids, and fat-soluble vitamins such as A, E, and K. They are also involved in cell metabolism.
  • What is a readily available natural source for extracting polyprenols?: Live conifer needles are identified as one of the richest and most widely available natural sources for extracting polyprenols. Commercial extraction methods are designed to preserve the biological activity of these compounds.

Prenol is found naturally in which of the following?

Answer: Various fruits like citrus and berries, and plants like tomato and coffee

Prenol occurs naturally in a variety of plant sources, including citrus fruits, berries, tomato, and coffee plants, demonstrating its presence in diverse ecosystems.

Related Concepts:

  • What is Prenol, and where does it occur naturally?: Prenol, also known as 3-methyl-2-buten-1-ol, is a natural alcohol and one of the simplest terpenoids. It is found naturally in various fruits (e.g., citrus, berries) and plants (e.g., tomato, coffee).
  • Which companies are known to manufacture Prenol industrially?: Prenol is manufactured industrially by companies such as BASF in Germany and Kuraray in Asia. These companies produce it as an intermediate for pharmaceuticals and aroma compounds.
  • How does Prenol relate to the concept of 'isoprenols'?: Prenol is considered one of the simplest terpenoids and is a building block for isoprenoid alcohols, which are sometimes referred to as 'isoprenols' due to their structural relation to isoprene units. However, it is important not to confuse Prenol with its isomer, isoprenol (3-methyl-3-buten-1-ol).

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