Draw the structures of the following compounds:
$(i)$ $3-$Methylbutanal
$(ii)$ $p-$Nitropropiophenone
$(iii)$ $p-$Methylbenzaldehyde
$(iv)$ $4-$Methylpent$-3-$en$-2-$one
$(v)$ $4-$Chloropentan$-2-$one
$(vi)$ $3-$Bromo$-4-$phenylpentanoic acid
$(vii)$ $p, p^{\prime}-$Dihydroxybenzophenone
$(viii)$ Hex$-2-$en$-4-$ynoic acid

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(N/A) $(i)$ $(CH_3)_2CHCH_2CHO$
$(ii)$ $O_2NC_6H_4COCH_2CH_3$
$(iii)$ $CH_3C_6H_4CHO$
$(iv)$ $CH_3COCH=C(CH_3)_2$
$(v)$ $CH_3COCH_2CH(Cl)CH_3$
$(vi)$ $CH_3CH(C_6H_5)CH(Br)CH_2COOH$
$(vii)$ $HOC_6H_4COC_6H_4OH$
$(viii)$ $CH_3C \equiv CCH=CHCOOH$

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What are $\underline{A}, \underline{B}, \underline{C}$ in the following reactions?
$(I)$ $(CH_3 CO_2)_2 Ca \stackrel{\Delta}{\longrightarrow} \underline{A}$
$(II)$ $CH_3 CO_2 H \underset{\text{Red P}}{\stackrel{HI}{\longrightarrow}} \underline{B}$
$(III)$ $2 CH_3 CO_2 H \stackrel{P_4 O_{10}}{\longrightarrow} \underline{C}$
$\underline{A} \quad \underline{B} \quad \underline{C}$

An organic acid $P$ $(C_{11}H_{12}O_2)$ can easily be oxidized to a dibasic acid which reacts with ethylene glycol to produce a polymer,dacron. Upon ozonolysis,$P$ gives an aliphatic ketone as one of the products. $P$ undergoes the following reaction sequences to furnish $R$ via $Q$. The compound $P$ also undergoes another set of reactions to produce $S$.
$(1)$ The compound $R$ is
$(2)$ The compound $S$ is
Give the answer for questions $(1)$ and $(2)$.

In the following reaction,$X$ and $Y$ are respectively
$CH_3 COOH + NH_3$ $\longrightarrow X \stackrel{\Delta}{}$ ${\longrightarrow} Y + H_2 O$

Which of the following represents the decreasing order of reactivity towards reaction with ammonia?

How many products will be formed when the given compound undergoes decarboxylation?

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