MCQ
In which alkyl halide, $S{N^2}$ mechanism is favoured maximum
- ✓$C{H_3}Cl$
- B$C{H_3}C{H_2}Cl$
- C${(C{H_3})_2}CHCl$
- D${(C{H_3})_3}C - Cl$
${S_{{N^1}}}$ Substitution nucleophilic unimolecular order of different alkyl halides , ${3^o} > {2^o} > {1^o}$.
Generate a complete, print-ready paper with questions like this in minutes — across 16+ boards, with answer keys.
(Image)
Pre-exponential factors for the forward and backward reactions are $10^{15} \mathrm{~s}^{-1}$ and $10^{11} \mathrm{~s}^{-1}$, respectively. If the value of $\log \mathrm{K}$ for the reaction at $500 \mathrm{~K}$ is $6$ , the value of $\left|\log \mathrm{k}_{\mathrm{b}}\right|$ at $250 \mathrm{~K}$ is $\qquad$
$[\mathrm{K}=$ equilibrium constant of the reaction
$\mathrm{k}_{\mathrm{f}}=$ rate constant of forward reaction
$\mathrm{k}_{\mathrm{b}}=$ rate constant of backward reaction]

