The enol percentage of the following compound is maximum for:
- A$CH_3-CO-CH_2-CO-CH_3$
- BCyclohexane$-1,2-$dione
- CCyclohexa$-2,4-$dien$-1-$one
- D$CH_3-CO-CH_2-CO-OC_2H_5$
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Similar Questions
How many transition states and intermediates will be formed during the course of the following reaction?
Medium
View SolutionThe products $(A)$ and $(B)$ of the above reaction are:
Difficult
View SolutionMatch the reactions in Column-$(I)$ with the type of reaction mechanism in Column-$(II)$.
Column-$(I)$ (Reaction) Column-$(II)$ (Type of Reaction) $(A)$ $\text{Cyclohexene} + Br_2 \xrightarrow{\Delta, uv} \text{3-Bromocyclohexene}$ $(i)$ $\text{Nucleophilic substitution}$ $(B)$ $\text{4-Hydroxybenzyl alcohol} + HCl \xrightarrow{\Delta} \text{4-Hydroxybenzyl chloride}$ $(ii)$ $\text{Electrophilic addition}$ $(C)$ $\text{Cyclohexene} + Br_2 \xrightarrow{CCl_4} \text{1,2-Dibromocyclohexane}$ $(iii)$ $\text{Free radical substitution}$ $(D)$ $\text{Toluene} + Cl_2 \xrightarrow{Fe, \text{dark}} \text{o/p-Chlorotoluene}$ $(iv)$ $\text{Electrophilic aromatic substitution}$
| Column-$(I)$ (Reaction) | Column-$(II)$ (Type of Reaction) |
|---|---|
| $(A)$ $\text{Cyclohexene} + Br_2 \xrightarrow{\Delta, uv} \text{3-Bromocyclohexene}$ | $(i)$ $\text{Nucleophilic substitution}$ |
| $(B)$ $\text{4-Hydroxybenzyl alcohol} + HCl \xrightarrow{\Delta} \text{4-Hydroxybenzyl chloride}$ | $(ii)$ $\text{Electrophilic addition}$ |
| $(C)$ $\text{Cyclohexene} + Br_2 \xrightarrow{CCl_4} \text{1,2-Dibromocyclohexane}$ | $(iii)$ $\text{Free radical substitution}$ |
| $(D)$ $\text{Toluene} + Cl_2 \xrightarrow{Fe, \text{dark}} \text{o/p-Chlorotoluene}$ | $(iv)$ $\text{Electrophilic aromatic substitution}$ |
Medium
View SolutionThe alkene formed as a major product in the below elimination reaction is
MediumAIEEE 2006
View SolutionBased on the provided energy profile diagram,transition state $2$ $(T.S. 2)$ is structurally most likely similar to which of the following?
Medium
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