$A$ solution of $(\pm)-2$-chloro-$2$-phenylethane in toluene is mixed slowly with a small amount of $SbCl_5$. The reaction proceeds due to the formation of:
- ACarbanion
- BCarbene
- CFree radical
- DCarbocation
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Similar Questions
Which compound might be synthesized by the $S_N2$ displacement of an alkyl-halide?
Medium
View SolutionMatch the following:
Reactants Products $A$. $C_2H_5Cl$,moist $Ag_2O$ $I$. $CH_3CH_2ONO$ $B$. $C_2H_5Cl$,aqueous ethanolic $AgCN$ $II$. $C_2H_4$ $C$. $C_2H_5Cl$,aqueous ethanolic $AgNO_2$ $III$. $CH_3CH_2OH$ $D$. $C_2H_5Cl$,ethanolic $KOH$ $IV$. $CH_3CH_2NC$
The correct match is:
| Reactants | Products |
|---|---|
| $A$. $C_2H_5Cl$,moist $Ag_2O$ | $I$. $CH_3CH_2ONO$ |
| $B$. $C_2H_5Cl$,aqueous ethanolic $AgCN$ | $II$. $C_2H_4$ |
| $C$. $C_2H_5Cl$,aqueous ethanolic $AgNO_2$ | $III$. $CH_3CH_2OH$ |
| $D$. $C_2H_5Cl$,ethanolic $KOH$ | $IV$. $CH_3CH_2NC$ |
The correct match is:
What is the major product obtained in the following reaction?
Medium
View SolutionWhich of the following compounds will undergo $S_{N^1}$ reaction most easily?
Difficult
View SolutionDehydrohalogenation of an alkyl halide is a/an
Medium
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