What happends when an optically active alkyl halide undergoes nucelophilic substitution?

Alkanes undergo free radical substitution, aromatic compounds undergo electrophilic substitution and alkyl halides undergo nucleophilic substitution reactions

Aryl halides are less reactive than alkyl halides due to the presence partial double character of C - X bond in aryl halides. Arly halides undergo nucleophilic substitution reactions, if electron withdrawing groups are introduced in ortho & para - positions in aryl halides. The reaction mechanism involves two steps. Keeping these points in view answer the following questions. Which of the following is the correct order of reactivity of the aryl halides with a given nucleophile

Aryl halides are less reactive than alkyl halides due to the presence partial double character of C - X bond in aryl halides. Arly halides undergo nucleophilic substitution reactions, if electron withdrawing groups are introduced in ortho & para - positions in aryl halides. The reaction mechanism involves two steps. Keeping these points in view answer the following questions. The number of resonance structure possible for chlorobenzene is

The nucleophilic substitution reactions taking place in aromatic system are designated as SN Ar In fact aryl halides do not easily undergo nucleophilic substitution under ordinary conditions. However, introduction of electron- withdrawing groups in o, p – positions makes the reaction to go faster. Keeping these general points in view answer the following questions product. The solution is treated with AgNO_3 solution. Which of the following is correct

The nucleophilic substitution reactions taking place in aromatic system are designated as SN Ar In fact aryl halides do not easily undergo nucleophilic substitution under ordinary conditions. However, introduction of electron- withdrawing groups in o, p – positions makes the reaction to go faster. Keeping these general points in view answer the following questions Which of the following structures is correct in the mechanism of the reaction

Aryl halides are less reactive than alkyl halides due to the presence partial double character of C - X bond in aryl halides. Arly halides undergo nucleophilic substitution reactions, if electron withdrawing groups are introduced in ortho & para - positions in aryl halides. The reaction mechanism involves two steps. Keeping these points in view answer the following questions. Which compound undergo nucleophilic substitution under mild conditions

Which of the following statements is correct for optically active alkyl halides, upon reaction with nucleophiles ?

A dextrorotatory optically active alkyl halide undergoes hydrolysis by S_N2 mechanism. The resulting alcohol is.