Which of the following alcohols would undergo Sn2 substitution to an alkyl halide (using HBr) the...
Which of the following alcohols would undergo Sn2 substitution to an alkyl halide (using HBr) the fastest? Explain.
CH3CH2CH(OH)CH3b. CH3CH2CH2OHc. (CH3)3COH
Homework Answers
answer is
b. CH3CH2CH2OH
because sterically free as compared to seconadr and tertiary alcohol.due to stericlly free ,the nucleophile can easily attacks from back side while leavig the OH^-1 from front side. that is posible only in primary alcohol.
so b .CH3CH2CH2OH is a primary alcohol so is very fast react towards SN^2 REACTION.
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Which of the following alcohols would undergo Sn2 substitution
to an alkyl halide (using HBr) the...
Which of the following alkyl halide will not undergo Sul or Sn2 reaction?
Which of the following alkyl halide will not undergo Sul or Sn2 reaction?
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Which of the following alkyl halide will not undergo
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11. Which of the following alkyl halides will undergo the fastest SN2 reaction? < <===- ய
11. Which of the following alkyl halides will undergo the fastest SN2 reaction? < <===- ய
Which alkyl halide shown below would react the fastest under typical SN2 conditions?
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bimolecular nucleophilic substitution (SN2) reaction in which
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theelectrophile. Is triphenylphosphine acting like a Lewis acid,
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Alcohol undergo substitution to form alkyl halides. HBr, SOCL2, and PBr3 are reagents used in these...
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PA
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theelectrophile. Is triphenylphosphine acting like a Lewis acid,
Lewis base, Bronsted-Lowry acid, orBronsted-Lowry base? How would
you characterize the behavior of the alkyl halide?
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benzyltriphenylphosphonium bromide with sodium hydroxide. How would
you characterize this reaction?
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Alcohol undergo substitution to form alkyl halides. HBr, SOCL2, and PBr3 are reagents used in these reactions. Which reagent would you use in each reaction? Give reasons.
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