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Ch. 18 - Ketones and Aldehydes
Wade - Organic Chemistry 9th Edition
Wade9th EditionOrganic ChemistryISBN: 9780135213728당신이 사용하는 게 아니라요?교과서 변경
18장, 문제 54f

Predict the products formed when cyclohexanecarbaldehyde reacts with the following reagents.
(f) zinc amalgam and dilute hydrochloric acid

검증된 단계별 안내
1
Identify the functional group in cyclohexanecarbaldehyde. The molecule contains an aldehyde group (-CHO) attached to a cyclohexane ring.
Understand the role of zinc amalgam and dilute hydrochloric acid. This combination is used in the Clemmensen reduction, which reduces aldehydes and ketones to their corresponding alkanes.
In the Clemmensen reduction, the aldehyde group (-CHO) is reduced to a -CH3 group. This involves the removal of the oxygen atom from the aldehyde and the addition of two hydrogen atoms.
Write the reaction mechanism conceptually: The aldehyde group undergoes reduction in the presence of zinc amalgam and HCl, resulting in the formation of cyclohexane with a methyl group attached (cyclohexylmethane).
Verify the product structure: The aldehyde group is completely reduced, and no other functional groups are present in the molecule. The final product is cyclohexylmethane.

비슷한 문제에 대한 검증된 영상 답변:

이 영상 해법은 위 문제에 도움이 된다고 튜터들이 추천한 것입니다.
영상 길이:
3m
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주요 개념

질문에 올바르게 답하기 위해 반드시 이해해야 하는 핵심 개념들은 다음과 같습니다.

Wurtz Reaction

The Wurtz reaction involves the reduction of carbonyl compounds using zinc amalgam in the presence of an acid. In this context, cyclohexanecarbaldehyde is reduced to form cyclohexylmethanol. This reaction is significant in organic synthesis for converting aldehydes and ketones into alcohols.
추천 영상:
05:09
Heck Reaction

Reduction Reactions

Reduction reactions in organic chemistry refer to the gain of electrons or decrease in oxidation state by a molecule. In the case of cyclohexanecarbaldehyde, the carbonyl group (C=O) is reduced to a hydroxyl group (C-OH), resulting in the formation of an alcohol. Understanding reduction mechanisms is crucial for predicting product formation.
추천 영상:
07:12
Reductive Amination

Aldehyde Reactivity

Aldehydes are highly reactive due to the presence of the carbonyl group, which is polarized and susceptible to nucleophilic attack. In the reaction with zinc amalgam and dilute hydrochloric acid, the aldehyde undergoes reduction, highlighting its reactivity compared to other functional groups. Recognizing the behavior of aldehydes is essential for predicting reaction outcomes.
추천 영상:
01:34
Name the aldehyde