Which alkyl halide reacts fastest (or slowest) by SN1 or SN2

1. A.
   (a)
2. B.
   (b)
3. C.
   (c)
4. D.
   (d)

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1. A.
   n-Butyl iodide
2. B.
   sec-butyl iodide
3. C.
   Isobutyl iodide
4. D.
   tert-Butyl iodide

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1. A.
   $\mathrm{(CH_3)_3C\text{-}F}$
2. B.
   $\mathrm{(CH_3)_3C\text{-}Cl}$
3. C.
   $\mathrm{(CH_3)_3C\text{-}Br}$
4. D.
   $\mathrm{(CH_3)_3C\text{-}I}$

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1. A.
   $\mathrm{CH_3\text{-}Br}$
2. B.
   $\mathrm{(CH_3)_3C\text{-}Br}$
3. C.
   $\mathrm{CH_3\text{-}CH_2\text{-}Br}$
4. D.
   $\mathrm{(CH_3)_2CH\text{-}Br}$

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1. A.
   Methyl chloride
2. B.
   Chloroethane
3. C.
   1-Chlorobutane
4. D.
   Tertiary Butyl chloride

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1. A.
   $\mathrm{CH_3Br}$
2. B.
   $\mathrm{C_2H_5Br}$
3. C.
   $\mathrm{(CH_3)_3C{-}Br}$
4. D.
   $\mathrm{CH_3CH_2CH_2Br}$

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1. A.
   $\mathrm{CH_3Br}$
2. B.
   $\mathrm{(CH_3)_3C{-}Br}$
3. C.
   $\mathrm{(CH_3)_2CH{-}Br}$
4. D.
   $\mathrm{CH_3CH_2Br}$

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