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Trans-1-2-dimethylcyclohexane...

Trans-1-2-dimethylcyclohexane

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Trans-1-2-dimethylcyclobutane

Cis-1,2-dimethylcyclohexane

Knowledge Check

  • The most stable from trans-1,2-dimethyl cyclohexane is:

    A
    (a) (1e, 2e)
    B
    (b) (1a, 2a)
    C
    (c) (1e, 2a)
    D
    (d) (1a, 2e)
  • The stable form of trans-1,4-dimethylcylohexane is represented as:

    A
    B
    C
    D
  • The stable conformer (s) of trans -1-4- dimethyl] cyclohexane is/are:

    A
    `1-` axial -`4-` equatorial form
    B
    `1-` axial `-4-` axial form
    C
    `1-` equatorial `-4-` axial from
    D
    `1-` equatorial`-4-` equatorial from
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    Which is more stable, cis - or trans-1,2-dimethyl cyclobutane and whyh?

    Draw the most stable conformation of (a) 1,2-dimethylcyclohexane, (b) cyclohexane-1,3-diol

    The number of chiral carbon atoms in I, II , III respectively are I. 1,2-dimethylcyclohexane II. 2-methylpentane (iii) 3-methylhexane

    The most stable conformational isomer of trans-1-ethyl-2-methylcyclohexane will be

    Given three compounds X, Y, Z as 1, 2, dimethylcyclohexane (X), 4-methyl cyclopentene (Y) and 3-methylcyclohexene (Z). The number of chiral carbon atoms in X, Y, Z would respectively be