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15.5.8: Chapter 8

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    482462
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    Problem 8-1 2-Methyl-2-butene and 2-methyl-1-butene
    Problem 8-3 trans-1,2-Dichloro-1,2-dimethylcyclohexane
    Problem 8-5 trans-2-Bromocyclopentanol
    Problem 8-6 Markovnikov
    Problem 8-7
    (a) 2-Pentanol
    (b) 2-Methyl-2-pentanol
    Problem 8-8
    (a) Oxymercuration of 2-methyl-1-hexene or 2-methyl-2-hexene
    (b) Oxymercuration of cyclohexylethylene or hydroboration of ethylidenecyclohexane
    Problem 8-9
    (a) The condensed structural formula has a 5-carbon chain. C2 is bonded to a methyl group. C3 is bonded to a hydroxyl group.
    (b) The structure has a cyclohexane ring bonded to a 2-carbon chain with a hydroxyl group bonded to C1  ring attachment.
    Problem 8-10
    (a) 3-Methyl-1-butene
    (b) 2-Methyl-2-butene
    (c) Methylenecyclohexane
    Problem 8-12
    (a) 2-Methylpentane
    (b) 1,1-Dimethylcyclopentane
    (c) tert-Butylcyclohexane
    Problem 8-14
    (a) 1-Methylcyclohexene
    (b) 2-Methyl-2-pentene
    (c) 1,3-Butadiene
    Problem 8-15
    (a) CH3COCH2CH2CH2CH2CO2H
    (b) CH3COCH2CH2CH2CH2CHO
    Problem 8-16
    (a) 2-Methylpropene
    (b) 3-Hexene
    Problem 8-17
    (a) The structure has a cyclohexane ring fused to C2 of a cyclopropane ring, in which C1 of the cyclopropyl ring is bonded to two chlorine atoms.
    (b) The condensed structure has a 6-carbon chain. C2 and C3 are bonded to a common methylene group. C5 is bonded to a methyl group.
    Problem 8-18
    (a) H2C ═ CHOCH3
    (b) ClCH ═ CHCl
    Problem 8-20

    An optically inactive, non-50 : 50 mixture of two racemic pairs: (2R,4R) + (2S,4S) and (2R,4S) + (2S,4R)

    Problem 8-21 Non-50 : 50 mixture of two racemic pairs: (1S,3R) + (1R,3S) and (1S,3S) + (1R,3R)

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