$A$ solution of $D(+)-1-$chloro$-1-$phenylethane in toluene racemises slowly in the presence of a small amount of $SbCl_5$,due to the formation of:

  • A
    Carbanion
  • B
    Carbene
  • C
    Free radical
  • D
    Carbocation

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Similar Questions

Consider the following reaction:
$CH_3-CH_2-CH(Br)-CH_3 \xrightarrow{alc. KOH, \Delta} CH_3-CH_2-CH=CH_2 (I) + CH_3-CH=CH-CH_3 (II)$
Which of the following statements are correct?
$a.$ $I$ is the major product of the reaction
$b.$ $II$ is the major product of the reaction
$c.$ Formation of $I$ is in accordance with Saytzeff's rule
$d.$ $II$ is more stable because it is more substituted

Write about the $\beta$-elimination reactions of haloalkane compounds.

Difficult
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The best method for the preparation of $Me_{3}CCN$ is

$1-$chloro$-3-$methylbutane on reaction with zinc and dilute hydrochloric acid gives . . . . . . as the major product.

Match the following reactions with their mechanisms:
$(A)$ $CH_3CH_2CH_2I \xrightarrow{aq. KOH}$
$(B)$ $(CH_3)_3CCl \xrightarrow{H_2O}$
$(I)$ $S_N1$
$(II)$ $E_2$
$(III)$ $S_N2$
$(IV)$ $E_1$

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