Predict the major product of the following reaction:
$1,3$-benzodioxole $\xrightarrow[(ii) CHCl_3, NaOH]{(i) HI \text{ (excess)}}$ ?

For the given reaction,find the sum of $x + y = ?$
$CH_3-CH_2-CO-CH_3 \xrightarrow[(ii) \ y \ mol \ NaNH_2]{(i) \ x \ mol \ PCl_5} CH_3-C \equiv C-CH_3$

Given below are the four isomeric compounds $(P, Q, R, S)$. Identify the correct statements from below.
$A$. $Q, R$ and $S$ will give a precipitate with $2,4-DNP$.
$B$. $P$ and $Q$ will give a positive Bayer's test.
$C$. $Q$ and $R$ will give a sooty flame.
$D$. $R$ and $S$ will give a yellow precipitate with $I_2/NaOH$.
$E$. $Q$ alone will deposit silver with Tollen's reagent.
Choose the correct option.

Match List-$I$ with List-$II$.
List-$I$ (Reaction):
$A$. Bicyclohexylidene $\rightarrow$ $2$ Cyclohexanone
$B$. Benzene $\rightarrow$ Benzophenone
$C$. Cyclohexanol $\rightarrow$ Cyclohexanone
$D$. Ethylbenzene $\rightarrow$ Potassium benzoate
List-$II$ (Reagents/Condition):
$I$. Benzoyl chloride / Anhydrous $AlCl_3$
$II$. $CrO_3$
$III$. $KMnO_4 / KOH, \Delta$
$IV$. $(i) O_3, (ii) Zn-H_2O$
Choose the correct answer from the options given below:

The product of the given reaction is:

An ester $(A)$ with molecular formula $C_9H_{10}O_2$ was treated with excess of $CH_3MgBr$ and the complex so formed was treated with $H_2SO_4$ to give an olefin $(B)$. Ozonolysis of $(B)$ gave a ketone with molecular formula $C_8H_8O$ which shows positive iodoform test. The structure of $(A)$ is