Does weed still have the same effects when put in food or drinks?
1 answer:
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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.
Answer:
0.0010 mol·L⁻¹s⁻¹
Explanation:
Assume the rate law is
rate = k[A][B]²
If you are comparing two rates,
You are cutting each concentration in half, so
Then,