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    Carbocations - Practice Questions & MCQ

    Edited By admin | Updated on Sep 18, 2023 18:35 AM | #JEE Main

    Quick Facts

    • Carbocations is considered one the most difficult concept.

    • 40 Questions around this concept.

    Solve by difficulty

    The shape of carbocation is 

    The total number of optically active compounds formed in the following reaction is :

    The order of stability of the following carbocations:

            is :

    Which of the following carbocations is most stable?

    The correct stability order of carbocations is

    The correct order of stability of the carbocations is 

     

     

     

    Which is the most stable carbocation

     

    The stability of carbocations

    ${ }_{(1)}\left(\mathrm{CH}_3\right)_3 \mathrm{C}^{\oplus}$                      (II) $\left(\mathrm{CH}_3\right)_2 \mathrm{C}^{\oplus}\left(\mathrm{OCH}_3\right)$                                                                        

    (III) $\mathrm{CH}_3 \mathrm{CH}_2 \mathrm{CH}_2 \mathrm{C}^{\oplus} \mathrm{H}_2$       (Iv) $\mathrm{CH}_3 \mathrm{C}^{\oplus} \mathrm{HCH}_2 \mathrm{CH}_3$

    follows the order

    Which one of the carbocations from the following
    is most stable ?

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    What is the correct order of decreasing stability of the following cations?

    Concepts Covered - 1

    Carbocations

    A species having a carbon atom possessing a sextet (6 in a group) of electrons and a positive charge is called a carbocation (earlier called carbonium ion). The +CHion is known as a methyl cation or methyl carbonium ion. Carbocations are classified as primary, secondary or tertiary depending on whether one, two or three carbons are directly attached to the positively charged carbon. Carbocations are highly unstable and reactive species. Alkyl groups directly attached to the positively charged carbon stabilise the carbocations due to inductive and hyperconjugation effects. The observed order of carbocation stability is: +CH3 < CH3C+H2 < (CH3)2C+H < (CH3)3C+. These carbocations have a trigonal planar shape with positively charged carbon being sp2 hybridised. Thus, the shape of +CH3 may be considered as being derived from the overlap of three equivalent C(sp2) hybridised orbitals with 1s orbital of each of the three hydrogen atoms. Each bond may be represented as C(sp2)–H(1s) sigma bond. The remaining carbon orbital is perpendicular to the molecular plane and contains no electrons. The shape of methyl carbocation is given as below:

                                                                                               

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    Carbocations

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    Reference Books

    Carbocations

    Chemistry Part II Textbook for Class XI

    Page No. : 349

    Line : 22

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