14. The final solution contains
(A) $\left[ \mathrm { Pb } \left( \mathrm { NH } _ { 3 } \right) _ { 4 } \right] ^ { 2 + }$ and $\left[ \mathrm { CoCl } _ { 4 } \right] ^ { 2 - }$
(B) $\left[ \mathrm { Al } \left( \mathrm { NH } _ { 3 } \right) _ { 4 } \right] ^ { 3 + }$ and $\left[ \mathrm { Cu } \left( \mathrm { NH } _ { 3 } \right) _ { 4 } \right] ^ { 2 + }$
(C) $\left[ \mathrm { Ag } \left( \mathrm { NH } _ { 3 } \right) _ { 2 } \right] ^ { + }$and $\left[ \mathrm { Cu } \left( \mathrm { NH } _ { 3 } \right) _ { 4 } \right] ^ { 2 + }$
(D) $\left[ \mathrm { Ag } \left( \mathrm { NH } _ { 3 } \right) _ { 2 } \right] ^ { + }$and $\left[ \mathrm { Ni } \left( \mathrm { NH } _ { 3 } \right) _ { 6 } \right] ^ { 2 + }$
ANSWER: C
Paragraph for Question Nos. 15 and 16
An acyclic hydrocarbon $\mathbf { P }$, having molecular formula $\mathrm { C } _ { 6 } \mathrm { H } _ { 10 }$, gave acetone as the only organic product through the following sequence of reactions, in which $\mathbf { Q }$ is an intermediate organic compound.
(i) conc. $\mathrm { H } _ { 2 } \mathrm { SO } _ { 4 }$ (catalytic amount) $\left( \mathrm { C } _ { 6 } \mathrm { H } _ { 10 } \right)$
[Figure] [Figure] [Figure](ii) $\mathrm { NaBH } _ { 4 }$ /ethanol
(iii) dil. acid
(ii) $\mathrm { O } _ { 3 }$
(iii) $\mathrm { Zn } / \mathrm { H } _ { 2 } \mathrm { O }$