In the following reaction, 'A' is

Consider the above reaction and identify the product B.

The most stable carbocation for the following is:

In the above conversion of compound $(\mathrm{X})$ to product $(\mathrm{Y})$, the sequence of reagents to be used will be:

Benzyl isocyanide can be obtained by : A. B. C. D. Choose the correct answer from the options given below :

Reaction of propanamide with $$\mathrm{B}{\mathrm{r}}_2/KOH(\mathrm{aq})$$ produces :

The major product 'P' for the following sequence of reactions is :

Match List I with List II .tg {border-collapse:collapse;border-spacing:0;} .tg td{border-color:black;border-style:solid;border-width:1px;font-family:Arial, sans-serif;font-size:14px; overflow:hidden;padding:10px 5px;word-break:normal;} .tg th{border-color:black;border-style:solid;border-width:1px;font-family:Arial, sans-serif;font-size:14px; font-weight:normal;overflow:hidden;padding:10px 5px;word-break:normal;} .tg .tg-baqh{text-align:center;vertical-align:top} .tg .tg-7btt{border-color:inherit;font-weight:bold;text-align:center;vertical-align:top} .tg .tg-0pky{border-color:inherit;text-align:left;vertical-align:top} List I List II Reaction Reagents (A) Hoffmann Degradation (I) $$Conc.KOH$$, $$\Delta$$ (B) Clemenson reduction (II) $$\mathrm{CHC}{\mathrm{l}}_3,NaOH/{\mathrm{H}}_3\mathrm{O}$$$${}^{\oplus }$$ (C) Cannizaro reaction (III) $$\mathrm{B}{\mathrm{r}}_2,\mathrm{NaOH}$$ (D) Reimer-Tiemann Reaction (IV) $$\mathrm{Zn}-Hg/HCl$$ Choose the correct answer from the options given below :

Match List I with List II .tg {border-collapse:collapse;border-spacing:0;} .tg td{border-color:black;border-style:solid;border-width:1px;font-family:Arial, sans-serif;font-size:14px; overflow:hidden;padding:10px 5px;word-break:normal;} .tg th{border-color:black;border-style:solid;border-width:1px;font-family:Arial, sans-serif;font-size:14px; font-weight:normal;overflow:hidden;padding:10px 5px;word-break:normal;} .tg .tg-c3ow{border-color:inherit;text-align:center;vertical-align:top} .tg .tg-7btt{border-color:inherit;font-weight:bold;text-align:center;vertical-align:top} .tg .tg-0pky{border-color:inherit;text-align:left;vertical-align:top} List I (Amines) List II ($$\mathrm{p}{\mathrm{K}}_{\mathrm{b}}$$) A. Aniline I. 3.25 B. Ethanamine II. 3.00 C. N-Ethylethanamine III. 9.38 D. N, N-Diethylethanamine IV. 3.29 Choose the correct answer from the options given below :

Match List I with List II .tg {border-collapse:collapse;border-spacing:0;} .tg td{border-color:black;border-style:solid;border-width:1px;font-family:Arial, sans-serif;font-size:14px; overflow:hidden;padding:10px 5px;word-break:normal;} .tg th{border-color:black;border-style:solid;border-width:1px;font-family:Arial, sans-serif;font-size:14px; font-weight:normal;overflow:hidden;padding:10px 5px;word-break:normal;} .tg .tg-c3ow{border-color:inherit;text-align:center;vertical-align:top} .tg .tg-7btt{border-color:inherit;font-weight:bold;text-align:center;vertical-align:top} .tg .tg-0pky{border-color:inherit;text-align:left;vertical-align:top} List I Isomeric pairs List II Type of isomers A. Propanamine and N-Methylethanamine I. Metamers B. Hexan-2-one and Hexan-3-one II. Positional isomers C. Ethanamide and Hydroxyethanimine III. Functional isomers D. o-nitrophenol and p-nitrophenol IV. Tautomers Choose the correct answer from the options given below :

Given below are two statements : In the light of the above statements, choose the correct answer from the options given below:

Choose the correct colour of the product for the following reaction.

Given below are two statements: Statement I : Pure Aniline and other arylamines are usually colourless. Statement II : Arylamines get coloured on storage due to atmospheric reduction. In the light of the above statements, choose the most appropriate answer from the options given below :

Increasing order of stability of the resonance structures is : Choose the correct answer from the options given below :

Consider the following sequence of reactions: The product ' $\mathrm{B}$ ' is

Decreasing order of reactivity towards electrophilic substitution for the following compounds is :

Compound $$\mathrm{A}$$ from the following reaction sequence is:

Match List I with List II 1 - Bromopropane is reacted with reagents in List I to give product in List II .tg {border-collapse:collapse;border-spacing:0;} .tg td{border-color:black;border-style:solid;border-width:1px;font-family:Arial, sans-serif;font-size:14px; overflow:hidden;padding:10px 5px;word-break:normal;} .tg th{border-color:black;border-style:solid;border-width:1px;font-family:Arial, sans-serif;font-size:14px; font-weight:normal;overflow:hidden;padding:10px 5px;word-break:normal;} .tg .tg-baqh{text-align:center;vertical-align:top} .tg .tg-amwm{font-weight:bold;text-align:center;vertical-align:top} .tg .tg-0lax{text-align:left;vertical-align:top} LIST I - Reagent LIST II - Product A. $$\mathrm{KOH}$$ (alc) I. Nitrile B. $$\mathrm{KCN}$$ (alc) II. Ester C. $$\mathrm{AgN}{\mathrm{O}}_2$$ III. Alkene D. $${\mathrm{H}}_3\mathrm{CCOOAg}$$ IV. Nitroalkane Choose the correct answer from the options given below:

In the reaction given below 'B' is

The incorrect statement regarding the reaction given below is