Concept explainers
a.
Interpretation:
To identify the products are formed when 3-methyl-2-cyclohexenone reacts with each of the given reactant.
Concept introduction:
So many number of reactions are involved in the Carbonyl group. The carbonyl group is electrophilic nature; therefore, it undergoes nucleophilic addition reactions.
For example, carbonyl group reacts with Grignard reagent, it undergoes nucleophilic addition reactions and form unstable tetrahedral intermediate by the elimination of leaving group.
Addition of hydrogen ion to the carbonyl carbon to form alkoxide ion. By the protonation of alkoxide ion forms alcohol.
b.
Interpretation:
To identify the products are formed when 3-methyl-2-cyclohexenone reacts with each of the given reactant.
Concept introduction:
So many number of reactions are involved in the Carbonyl group. The carbonyl group is electrophilic nature; therefore, it undergoes nucleophilic addition reactions.
For example, carbonyl group reacts with Grignard reagent, it undergoes nucleophilic addition reactions and form unstable tetrahedral intermediate by the elimination of leaving group.
Addition of hydrogen ion to the carbonyl carbon to form alkoxide ion. By the protonation of alkoxide ion forms alcohol.
c.
Interpretation:
To identify the products are formed when 3-methyl-2-cyclohexenone reacts with each of the given reactant.
Concept introduction:
So many number of reactions are involved in the Carbonyl group. The carbonyl group is electrophilic nature; therefore, it undergoes nucleophilic addition reactions.
For example, carbonyl group reacts with Grignard reagent, it undergoes nucleophilic addition reactions and form unstable tetrahedral intermediate by the elimination of leaving group.
Addition of hydrogen ion to the carbonyl carbon to form alkoxide ion. By the protonation of alkoxide ion forms alcohol.
d.
Interpretation:
To identify the products are formed when 3-methyl-2-cyclohexenone reacts with each of the given reactant.
Concept introduction:
So many number of reactions are involved in the Carbonyl group. The carbonyl group is electrophilic nature; therefore, it undergoes nucleophilic addition reactions.
For example, carbonyl group reacts with Grignard reagent, it undergoes nucleophilic addition reactions and form unstable tetrahedral intermediate by the elimination of leaving group.
Addition of hydrogen ion to the carbonyl carbon to form alkoxide ion. By the protonation of alkoxide ion forms alcohol.
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Chapter 16 Solutions
Organic Chemistry (8th Edition)
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