1A Which of the following alkyl halides would react most slowly to give the product shown? A. (CH3)2CHCH2I B. (CH3)2CHCH

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1A
Which of the following alkyl halides would react most slowly to
give the product shown?

1a Which Of The Following Alkyl Halides Would React Most Slowly To Give The Product Shown A Ch3 2chch2i B Ch3 2chch 1 (3.99 KiB) Viewed 39 times

A. (CH3)2CHCH2I
B.
(CH3)2CHCH2CH2I
C.
(CH3)2CHCH2CH2Br
D. (CH3)2CHCH2Br
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1B
A chiral (S)-configuration alkyl halide of formula
C8H17Br reacts with H2O to
give a product, formula C8H18O, as a racemic
mixture.
Which of the following statements is true?
A. The reaction proceeds via an SN1 mechanism,
which involves a bimolecular transition-state species.
B. The reaction proceeds via an SN2 mechanism, which
involves a carbocation intermediate.
C. The reaction proceeds via an SN2 mechanism, which
involves a bimolecular transition-state species.
D. The reaction proceeds via an SN1 mechanism, which
involves a carbocation intermediate.
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1C
Which is correct?

1a Which Of The Following Alkyl Halides Would React Most Slowly To Give The Product Shown A Ch3 2chch2i B Ch3 2chch 2 (4.7 KiB) Viewed 39 times

A. The alcohol is the electrophile and the mechanism is
SN2
B. The alcohol is the nucleophile and the mechanism is
SN2
C. The alcohol is the electrophile and the mechanism is
SN1
D. The alcohol is the nucleophile and the mechanism is
SN1
(CH3)₂CHCH₂C=C ? (CH3)2CHCH₂C=CCH₂CH(CH3)2
SOH CH3CH₂Br х