What is the major product formed in the following reaction?

  • A
    $3-$iodophenylacetonitrile
  • B
    $3-$cyanophenylacetonitrile
  • C
    $4-$cyano$-3-$methylphenylacetonitrile
  • D
    $3-$chlorophenylacetonitrile

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Identify the compound $(C)$ in the following reaction sequence:
$\gamma$-butyrolactone $\xrightarrow[(ii) SOCl_2]{(i) HCl} (A)$ $\xrightarrow[AlCl_3]{Ph-H} (B)$ $\xrightarrow{KOH/MeOH} (C)$

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Among the given pairs,in which pair does the first compound react faster than the second compound in an $S_{N}1$ reaction?

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The following is a substitution reaction in which $-CN$ replaces $-Cl$:
$R-Cl \xrightarrow[\text{alcoholic}]{KCN, \Delta} R-CN + KCl$
To obtain propanenitrile,$R-Cl$ should be:

The major product of the following reaction is:

For the given reaction
$R_1-C(R)(X)-R_2 \xrightarrow{HOH} R_1-C(R)(OH)-R_2$
Which substrate will give maximum racemisation?

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