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C(6)H(5)CH(2)Cl + X rarr C(6)H(5)CH(2) N...

`C_(6)H_(5)CH_(2)Cl + X rarr C_(6)H_(5)CH_(2) NH_(2) + Y`
The compounds X and Y are

A

`"HNO"_(3)` and HCl

B

`NH_(3)` and HCl

C

`HNO_(2) and H_(2)O`

D

none of these

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The correct Answer is:
To solve the question, we need to identify the compounds X and Y in the reaction: \[ C_6H_5CH_2Cl + X \rightarrow C_6H_5CH_2NH_2 + Y \] ### Step 1: Identify the Reactants and Products The reactant is benzyl chloride (\(C_6H_5CH_2Cl\)), and the product is benzylamine (\(C_6H_5CH_2NH_2\)). ### Step 2: Understand the Reaction Mechanism In this reaction, the chlorine atom in benzyl chloride is replaced by an amino group (\(-NH_2\)). This type of reaction is typically a nucleophilic substitution reaction, where the nucleophile attacks the carbon atom bonded to the chlorine, leading to the displacement of the chlorine atom. ### Step 3: Identify the Nucleophile The nucleophile in this reaction is likely ammonia (\(NH_3\)). Ammonia can donate a lone pair of electrons to the carbon atom, allowing it to form a bond with the nitrogen atom and replace the chlorine atom. ### Step 4: Determine the By-product When the chlorine atom leaves, it forms a chloride ion (\(Cl^-\)). Additionally, since the reaction involves the formation of a proton (\(H^+\)) from the ammonia, the by-product Y is hydrochloric acid (\(HCl\)). ### Step 5: Write the Final Reaction Combining all the information, we can summarize the reaction as follows: \[ C_6H_5CH_2Cl + NH_3 \rightarrow C_6H_5CH_2NH_2 + HCl \] From this, we can conclude: - \(X = NH_3\) (ammonia) - \(Y = HCl\) (hydrochloric acid) ### Final Answer - \(X = NH_3\) - \(Y = HCl\) ---
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VMC MODULES ENGLISH-HALOALKANES & HALOARENES -ENABLE
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