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Alkylhalides have polar C-X bond and und...

Alkylhalides have polar C-X bond and undergo nucleophilic substitution reactions. These give a variety of products with nucleophiles such as `-OH, -OR, -NH_(2), -CN, -NC, -NO_(2), -ONO, RCOO^(-)`, etc. They undergo mainly two types of nucleophilic substitution reactions, `S_(N)1` and `S_(N)2`. `S_(N)1` reactions are two steps reactions which proceed through the formation of carbocations while `S_(N)2` reactions are one step reaction which proceeds through the formation of transition state. The stability of carbocation and transition state determine the reactivity of alkyl halides.
Write the main products A and B in the following reaction.
`A overset(KNO_(2))larr CH_(3)CH_(2)Br overset(AgNO_(2))to B`.

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To solve the question, we need to analyze the reactions that occur when `CH3CH2Br` (ethyl bromide) is treated with `KNO2` and `AgNO2`. We will identify the main products A and B from these reactions. ### Step-by-Step Solution: 1. **Identify the Reactants**: The reactants are `CH3CH2Br` (ethyl bromide), `KNO2`, and `AgNO2`. 2. **Reaction with KNO2**: - When `CH3CH2Br` reacts with `KNO2`, the `K^+` ion is a spectator ion, while the `NO2^-` ion acts as a nucleophile. ...
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Alkylhalides have polar C-X bond and undergo nucleophilic substitution reactions. These give a variety of products with nucleophiles such as -OH, -OR, -NH_(2), -CN, -NC, -NO_(2), -ONO, RCOO^(-) , etc. They undergo mainly two types of nucleophilic substitution reactions, S_(N)1 and S_(N)2 . S_(N)1 reactions are two steps reactions which proceed through the formation of carbocations while S_(N)2 reactions are one step reaction which proceeds through the formation of transition state. The stability of carbocation and transition state determine the reactivity of alkyl halides. Which out of S_(N)1 or S_(N)2 results into inversion of configuration?

Alkylhalides have polar C-X bond and undergo nucleophilic substitution reactions. These give a variety of products with nucleophiles such as -OH, -OR, -NH_(2), -CN, -NC, -NO_(2), -ONO, RCOO^(-) , etc. They undergo mainly two types of nucleophilic substitution reactions, S_(N)1 and S_(N)2 . S_(N)1 reactions are two steps reactions which proceed through the formation of carbocations while S_(N)2 reactions are one step reaction which proceeds through the formation of transition state. The stability of carbocation and transition state determine the reactivity of alkyl halides. Which out of S_(N)1 or S_(N)2 results into inversion of configuration?

Knowledge Check

  • S_(N^(2)) mechanism proceeds through the formation of

    A
    Carbonium ion
    B
    Transition state
    C
    Free radical
    D
    Carbonion

  • S_(N)2 mechanism proceeds through formation of :

    A
    Carbonium ion
    B
    Transition state
    C
    Free radical
    D
    Carbanion

    • Similar Questions

    Explore conceptually related problems

    Alkylhalides have polar C-X bond and undergo nucleophilic substitution reactions. These give a variety of products with nucleophiles such as -OH, -OR, -NH_(2), -CN, -NC, -NO_(2), -ONO, RCOO^(-) , etc. They undergo mainly two types of nucleophilic substitution reactions, S_(N)1 and S_(N)2 . S_(N)1 reactions are two steps reactions which proceed through the formation of carbocations while S_(N)2 reactions are one step reaction which proceeds through the formation of transition state. The stability of carbocation and transition state determine the reactivity of alkyl halides. Arrange the following in the increasing order of reactivity towards S_(N)2 reaction:

    Alkylhalides have polar C-X bond and undergo nucleophilic substitution reactions. These give a variety of products with nucleophiles such as -OH, -OR, -NH_(2), -CN, -NC, -NO_(2), -ONO, RCOO^(-) , etc. They undergo mainly two types of nucleophilic substitution reactions, S_(N)1 and S_(N)2 . S_(N)1 reactions are two steps reactions which proceed through the formation of carbocations while S_(N)2 reactions are one step reaction which proceeds through the formation of transition state. The stability of carbocation and transition state determine the reactivity of alkyl halides. Arrange the following in the increasing order of reactivity towards S_(N)2 reaction:

    Alkylhalides have polar C-X bond and undergo nucleophilic substitution reactions. These give a variety of products with nucleophiles such as -OH, -OR, -NH_(2), -CN, -NC, -NO_(2), -ONO, RCOO^(-) , etc. They undergo mainly two types of nucleophilic substitution reactions, S_(N)1 and S_(N)2 . S_(N)1 reactions are two steps reactions which proceed through the formation of carbocations while S_(N)2 reactions are one step reaction which proceeds through the formation of transition state. The stability of carbocation and transition state determine the reactivity of alkyl halides. Complete the reaction: CH_(3)CH_(2)Br underset("Heat")overset(Ag_(2)O)to

    Alkylhalides have polar C-X bond and undergo nucleophilic substitution reactions. These give a variety of products with nucleophiles such as -OH, -OR, -NH_(2), -CN, -NC, -NO_(2), -ONO, RCOO^(-) , etc. They undergo mainly two types of nucleophilic substitution reactions, S_(N)1 and S_(N)2 . S_(N)1 reactions are two steps reactions which proceed through the formation of carbocations while S_(N)2 reactions are one step reaction which proceeds through the formation of transition state. The stability of carbocation and transition state determine the reactivity of alkyl halides. Complete the reaction: CH_(3)CH_(2)Br underset("Heat")overset(Ag_(2)O)to

    Alkylhalides have polar C-X bond and undergo nucleophilic substitution reactions. These give a variety of products with nucleophiles such as -OH, -OR, -NH_(2), -CN, -NC, -NO_(2), -ONO, RCOO^(-) , etc. They undergo mainly two types of nucleophilic substitution reactions, S_(N)1 and S_(N)2 . S_(N)1 reactions are two steps reactions which proceed through the formation of carbocations while S_(N)2 reactions are one step reaction which proceeds through the formation of transition state. The stability of carbocation and transition state determine the reactivity of alkyl halides. Write the structure of isomer of compound C_(4)H_(9)Br which is most reactive towards S_(N)1 reaction.

    Alkylhalides have polar C-X bond and undergo nucleophilic substitution reactions. These give a variety of products with nucleophiles such as -OH, -OR, -NH_(2), -CN, -NC, -NO_(2), -ONO, RCOO^(-) , etc. They undergo mainly two types of nucleophilic substitution reactions, S_(N)1 and S_(N)2 . S_(N)1 reactions are two steps reactions which proceed through the formation of carbocations while S_(N)2 reactions are one step reaction which proceeds through the formation of transition state. The stability of carbocation and transition state determine the reactivity of alkyl halides. Write the structure of isomer of compound C_(4)H_(9)Br which is most reactive towards S_(N)1 reaction.

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