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Ronch [10]
3 years ago
12

Which of the following alkyl halides will react fastest with CH3OH in an SN1 mechanism?

Chemistry
1 answer:
yaroslaw [1]3 years ago
5 0

Answer:

IV

Explanation:

The complete question is shown in the image attached.

Let us call to mind the fact  that the SN1 mechanism involves the formation of carbocation in the rate determining step. The order of stability of cabocations is; tertiary > secondary > primary > methyl.

Hence, a tertiary alkyl halide is more likely to undergo nucleophilic substitution reaction by SN1 mechanism since it forms a more stable cabocation in the rate determining step.

Structure IV is a tertiary alkyl halide, hence it is more likely to undergo nucleophilic  substitution reaction by SN1 mechanism.

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2 HI(g) ⇄ H2(g) + I2(g) Kc = 0.0156 at 400ºC 0.550 moles of HI are placed in a 2.00 L container and the system is allowed to rea
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<u>Answer:</u> The concentration of hydrogen gas at equilibrium is 0.0275 M

<u>Explanation:</u>

Molarity is calculated by using the equation:

\text{Molarity}=\frac{\text{Number of moles}}{\text{Volume of solution (in L)}}

Moles of HI = 0.550 moles

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\text{Initial concentration of HI}=\frac{0.550}{2}=0.275M

For the given chemical equation:

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<u>At eqllm:</u>           0.275-2x      x         x

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0.0156=\frac{x\times x}{(0.275-2x)^2}\\\\x=-0.0458,0.0275

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