Simun Mishra posted an Question
November 16, 2020 • 15:48 pm 30 points
  • IIT JAM
  • Chemistry (CY)

Can u pls explain me this question ?

2 Answer(s) Answer Now
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    Dinesh khalmaniya 1 Best Answer

    option B Alkynes are selectively converted into trans alkenes when they are reduced by a solution of sodium (or lithium) in liquid ammonia that contains stoichiometric amounts of an alcohol, such as ethanol.

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    sir pph3 = CH2 use for the reduction of ........?

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    wittig reaction

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    sir can u pls explain me only question I can't understand what the question ask

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    yes wait

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    can you share this question as a new query?

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    ok sir

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    Priyanshu kumar best-answer

    option B

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    but sir birch reduction is for conjugated alkyne and alkene na

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    I can't understand sir pls explain it

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    ok wait

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    ok sir and sir why not lindlar catalysts use here

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    simun here it is asked effective so Na /liq Nh3 give effective reduction

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    H2/lindlar catalyst always gives the cis-alkene, in contrast to Na/NH3, which gives the trans alkenes

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    Here trans alkene is asked so Na/Nh3 is used

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    which give cis alkene ?

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    H2/lindlar catalyst- cis alkene

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    but sir here no conjugation so how here negative charge and redical minimise the repulsion

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    check the mechanism simun

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    so sir all alkyne and alkene without conjugation also reduce to trans by this

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    and sir ph3p=CH2 is used for reducing of ?

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    this is wittig reagent ...you have read the mechanism of wittig reaction earlier

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    yes simun

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    tq sir

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    welcome and please accept the answer

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    ??

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