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Sourav posted an Question
August 29, 2020 โ€ข 23:01 pm 30 points
  • IIT JAM
  • Chemistry (CY)

According to me b is answer

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  • Suman Kumar

    So option D can't be correct benzyl Hydrogen is more acidic

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    See these were the reason given to me. So you will have to except it.

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    organic Chemistry padna koi aasan baat nahi hai ๐Ÿ˜„

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    true ๐Ÿ˜‚

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    i will give the same explanation if i become one of you guys next year.. ๐Ÿ˜‚

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    ๐Ÿ˜…

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    option C i will try to explain again with pen & paper at 9. please remind me

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    well sir you didn't give me explanation of why final temp in rev adiabatic exp is less than irr one.

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    ok both i will explain at night

  • Suman Kumar best-answer

    option A is correct

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    how

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    Is it correct

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    is it MSQ

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    no it is normal qs.. u r correct with ans

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    Sourav are you there

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    Actually I did the question by elimination method

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    explain

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    in option b -ve is more stable on smaller ring so b is not correct

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    in option c ist compound is extremely acidic. it is said that due to bulky methyl group oxygen shows -I effect

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    In option d you have sp2 hybridized phenyl ring which shows -M as well as -I effect

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    So option A is left

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    in option C both have - I effect due to O na?

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    in option C in ist compound O show -I effect as due to bulky methyl group it is no more planar. But in 2nd compound O show its usual nature of +M.

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    im not much convinced with your last explanation.. i think in option C both are equally acidic. but i guess in first option second molecule is more acidic because of less +I effect of methyl group due to distance

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    I agree with you Sourav.

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