12. Alcohols, Ethers, Epoxides and Thiols
Alcohol Nomenclature
12. Alcohols, Ethers, Epoxides and Thiols
Alcohol Nomenclature
We’ve learned how to name simple alcohols before, but now we are moving to polyols.
Note: I am moving away from the term glycol, and using polyols instead, since the term glycol is not specific enough.
1
concept
How to name polyols.
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In Summary:
Polyols with two hydroxyls are called diols, and polyols with three hydroxyls are called triols.
- Always give most priority to the –OH group.
2
example
Provide the correct common and IUPAC name.
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Note: The molecule should be named trans-1,3-cyclohexanediol.
There are other possible name variations that are also acceptable. Here are just a few:(R,R)-cyclohexane-1,3-diol, (1R, 3R)-1,3-cyclohexanediol

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example
Provide the correct common and IUPAC name.
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Do you want more practice?
We have more practice problems on Alcohol Nomenclature
Additional resources for Alcohol Nomenclature
PRACTICE PROBLEMS AND ACTIVITIES (11)
- Predict which member of each pair has the higher boiling point, and explain the reasons for your predictions. ...
- Predict which member of each pair will be more soluble in water. Explain the reasons for your answers. (a) hex...
- Draw the structures of the following compounds. (Includes both new and old names.) (d) 3-cyclopentylhexan-3-o...
- Give systematic (IUPAC) names for the following diols and phenols. (a) (b)
- Predict which member of each pair will be more acidic. Explain your answers. (d) 2,2-dichloropropan-1-ol or 2,...
- Predict which member of each pair will be more acidic. Explain your answers. (c) 2-chloroethanol or 2,2-dichlo...
- Predict which member of each pair is more acidic, and explain the reasons for your predictions. (b) cyclohexan...
- Predict which member of each pair is more acidic, and explain the reasons for your predictions. (a) cyclopenta...
- Which of the following bases would favorably deprotonate a hydroxyl group? (b) NaOH
- Which of the following bases would favorably deprotonate a hydroxyl group? (c) NaCN
- Which of the following bases would favorably deprotonate a hydroxyl group? (e)