The heterolytic cleavage of a carbon-chlorine bond gives:
- ATwo free radicals
- BTwo carbocations
- CTwo carbanions
- D$A$ carbocation and a chloride ion
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Similar Questions
In the reaction given below,the total number of atoms having $sp^2$ hybridization in the major product $P$ is. . . . .
What is the fission of a covalent bond? Explain its types with examples and the main differences.
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 SolutionWhich statement is correct for the given reactions?
Difficult
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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