Step 1: Definition of an ambident nucleophile
An ambident nucleophile is a nucleophile that can attack from two different atoms, leading to different products.
Step 2: Analyzing the given options \({CH}_3{O}^-\) (methoxide ion): Oxygen is the only nucleophilic site, so it is not ambident.
\({HO}^-\) (hydroxide ion): Only oxygen is nucleophilic, not ambident.
\({CH}_3{COO}^-\) (acetate ion): Resonance delocalization reduces the ambident character.
\({H}_2{O}\) (water): Oxygen is the only nucleophilic site, not ambident.
\({CN}^-\) (cyanide ion): - This ion has two nucleophilic centers: - The carbon (\(C\)) can perform nucleophilic attack (\(C\)-attack). - The nitrogen (\(N\)) can also attack (\(N\)-attack). - This makes it an ambident nucleophile.
Step 3: Conclusion Among the given options, only \({CN}^-\) is an ambident nucleophile. It can undergo nucleophilic substitution via both the carbon and nitrogen atoms.
In the Carius method of estimation of halogen, 0.4g of an organic compound gave 0.188g of AgBr. What is the percentage of bromine in the organic compound? (The atomic mass of Ag = 108 g mol\(^{-1}\) & Br = 80 g mol\(^{-1}\))
The IUPAC name of the complex \( [\text{Cr(NH}_3)_3(\text{H}_2\text{O})_3]\text{Cl}_3 \) is:
For the reaction:
\[ 2A + B \rightarrow 2C + D \]
The following kinetic data were obtained for three different experiments performed at the same temperature:
\[ \begin{array}{|c|c|c|c|} \hline \text{Experiment} & [A]_0 \, (\text{M}) & [B]_0 \, (\text{M}) & \text{Initial rate} \, (\text{M/s}) \\ \hline I & 0.10 & 0.10 & 0.10 \\ II & 0.20 & 0.10 & 0.40 \\ III & 0.20 & 0.20 & 0.40 \\ \hline \end{array} \]
The total order and order in [B] for the reaction are respectively: