Acetone reacts with iodine to form iodoform in the presence of

Which of the following reagents should be used to carry out the above conversion $:-$
(Image shows the reduction of a ketone group to a secondary alcohol in the presence of an ester group)

$HCDO \xrightarrow[{(50\%)}]{{OH^{-}}}$ Product of this Cannizzaro reaction is:

Which carbonyl group is most reactive for $NAR$ (Nucleophilic Addition Reaction)?

Which of the following is not true about acetophenone?

$(A)$ $\xrightarrow{NH_2OH} (B)$ $\xrightarrow{H_2SO_4} (C)$ $\xrightarrow{H_3O^{\oplus}} (D) + (E)$ $\xrightarrow{CHCl_3, KOH} CH_3-NC$ (carbylamine test). $(D)$ $\xrightarrow{SOCl_2} (F)$ $\xrightarrow{(i) PhMgBr \text{ (excess) } (ii) H^{\oplus}} (G)$ $\xrightarrow[\Delta]{H^{\oplus}} (H)$ $\xrightarrow{CH_2I_2, Zn/Cu} \text{1,1-diphenylcyclopropane}$. The molecular weight of compound $(A)$ is: