Chapter 21: Q9. (page 824)
Question: Which carbonyl group in each pair absorbs at a higher frequency?
a.
b.
Short Answer
Answer
a. (E)-but-2-enal absorbs at a higher frequency.
b. Cyclopropanone absorbs at a higher frequency
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Chapter 21: Q9. (page 824)
Question: Which carbonyl group in each pair absorbs at a higher frequency?
a.
b.
Answer
a. (E)-but-2-enal absorbs at a higher frequency.
b. Cyclopropanone absorbs at a higher frequency
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What reagents are needed to convert each compound into butanal (\({\bf{C}}{{\bf{H}}_{\bf{3}}}{\bf{C}}{{\bf{H}}_{\bf{2}}}{\bf{C}}{{\bf{H}}_{\bf{2}}}{\bf{CHO}}\))?
a.

b.

c.

Question: Give the structure corresponding to each name:
(a) sec-butyl ethyl ketone
(b) methyl vinyl ketone
(c) p-ethylacetophenone
(d) 3-benzoyl-2-benzylcyclopentanone
(e) 6,6-dimethylcyclohex-2-enone
(f) 3-ethylhex-5-enal
Question: Explain why benzaldehyde is less reactive than cyclohexanecarbaldehyde towards nucleophilic attack.

Question: The boiling point of butan-2-one ( 80 °C ) is significantly higher than the boiling point of diethyl ether (35 °C ), even though both compounds exhibit dipole–dipole interactions and have comparable molecular weights. Offer an explanation
Question: Give the IUPAC name for each aldehyde.
4. 3,6-diethylnonanal
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