Identify the final product $(D)$ in the following reaction sequence:
Phthalic anhydride $\xrightarrow{PCl_5} (A)$ $\xrightarrow{LiAlH_4} (B)$ $\xrightarrow{PCC} (C)$ $\xrightarrow{HO^-, \Delta} (D)$

An ester $(A)$ with molecular formula $C_9H_{10}O_2$ is reacted with an excess of $CH_3MgBr$. The resulting product is treated with concentrated $H_2SO_4$ to form an olefin $(B)$. Ozonolysis of $(B)$ yields a ketone with the formula $C_8H_8O$. What is the structure of $(A)$?

The increasing order of the acidity of the following carboxylic acids is:

Match the compounds given in Column-$I$ with their names in Column-$II$.

Column-$I$ (Formula)	Column-$II$ (Name)
$(A)$ $CH_3-CH=CHCHO$	$(i)$ $1,3$-diphenylprop-$2$-en-$1$-one
$(B)$ $CH_3-C(CH_3)=CH-COCH_3$	(ii) Acetophenone-$2,4$-dinitrophenylhydrazone
$(C)$ $C_6H_5-CH=CH-COC_6H_5$	(iii) But-$2$-enal
$(D)$ $C_6H_5-C(CH_3)=N-NH-C_6H_3(NO_2)_2$	(iv) $4$-methylpent-$3$-en-$2$-one

The ester among the following is

The products obtained in the given reactions are shown below. The number of possible products for $x$ and $y$ are: