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Chem&219 Unit 5 Questions and Correct Answers/ Latest Update / Already Graded

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Generic formula for alcohols Ans: R-OH phenol Ans: hydroxy-substituted aromatic molecules (any compound with an -OH attached to a benzene ring) IUPAC system rules for naming organic alcohols Ans: - organic alcohols are named by replacing the suffix of the parent chain of the molecule with the suffix -ol - The parent chain is numbered so as to give the hydroxyl group the lowest possible number. (examples: 1-propanol, and cyclohexanol) - with unsaturated alcohols the -ol suffix comes last and takes priority when numbering the parent chain (2-propene-1-ol) Page | 2 All rights reserved © 2025/ 2026 | - Molecules with more than one -OH group get a prefix describing the number of -OH groups added to the IUPAC name. (ethane-1,2-diol) Molecules with more than one -OH group Ans: polyols IUPAC rules for phenols Ans: - the suffix for an alcohol substituted benzene is "phenol" - start the numbering at the OH group (so OH is at the 1 position) (examples: phenol, 3-methylphenol, 2,4-dinitrophenol) Why can alcohols form strong hydrogen bonds? Ans: Due to the presence of the hydroxyl group, as the O-H bond is highly polarized by the electronegative oxygen atom. This polarization places a + charge on the hydrogen atom and a - charge on the oxygen atom. The polarization in the O-H bond on one alcohol molecule becomes attracted to the polarization in the O-H bond of another alcohol molecule. Page | 3 All rights reserved © 2025/ 2026 | Why do alcohols have much higher boiling points than other molecules of similar molecular weight? Ans: hydrogen bonding between alcohol molecules These attractions raise the amount of energy required to vaporize the liquid-phase molecules (boil), which translates into increased boiling point temperatures. Alcohol molecules can freely hydrogen bond to other molecules possessing what groups? Ans: O-H, N-H, or S-H functional groupings How does the water solubility of alcohol molecules change as the molecular weight changes? Ans: Alcohol molecules of lower molecular weight are mostly soluble in water as a result of the ability to hydrogen bond to OH, NH, or SH groups. As the molecular weight or carbon-chain length increases, the alcohol molecules become correspondingly less soluble in water. How do alcohols and phenols act as weak acids and weak bases? Page | 4

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2025/2026
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Page |1


Chem&219 Unit 5 Questions and Correct
Answers/ Latest Update / Already Graded
Generic formula for alcohols

Ans: R-OH


phenol

Ans: hydroxy-substituted aromatic molecules (any compound
with an -OH attached to a benzene ring)


IUPAC system rules for naming organic alcohols

Ans: - organic alcohols are named by replacing the suffix of the
parent chain of the molecule with the suffix -ol


- The parent chain is numbered so as to give the hydroxyl group
the lowest possible number. (examples: 1 -propanol, and
cyclohexanol)


- with unsaturated alcohols the -ol suffix comes last and takes
priority when numbering the parent chain (2-propene-1-ol)




All rights reserved © 2025/ 2026 |

, Page |2


- Molecules with more than one -OH group get a prefix
describing the number of -OH groups added to the IUPAC
name. (ethane-1,2-diol)


Molecules with more than one -OH group

Ans: polyols


IUPAC rules for phenols

Ans: - the suffix for an alcohol substituted benzene is "phenol"


- start the numbering at the OH group (so OH is at the 1
position)


(examples: phenol, 3-methylphenol, 2,4-dinitrophenol)


Why can alcohols form strong hydrogen bonds?

Ans: Due to the presence of the hydroxyl group, as the O -H
bond is highly polarized by the electronegative oxygen atom.
This polarization places a + charge on the hydrogen atom and a
- charge on the oxygen atom. The polarization in the O -H bond
on one alcohol molecule becomes attracted to the polarization
in the O-H bond of another alcohol molecule.


All rights reserved © 2025/ 2026 |

, Page |3



Why do alcohols have much higher boiling points than other molecules
of similar molecular weight?

Ans: hydrogen bonding between alcohol molecules


These attractions raise the amount of energy required to
vaporize the liquid-phase molecules (boil), which translates into
increased boiling point temperatures.


Alcohol molecules can freely hydrogen bond to other molecules
possessing what groups?

Ans: O-H, N-H, or S-H functional groupings


How does the water solubility of alcohol molecules change as the
molecular weight changes?

Ans: Alcohol molecules of lower molecular weight are mostly
soluble in water as a result of the ability to hydro gen bond to
OH, NH, or SH groups. As the molecular weight or carbon -chain
length increases, the alcohol molecules become
correspondingly less soluble in water.


How do alcohols and phenols act as weak acids and weak bases?



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