Answer:
Explanation:
Hello there!
In this case, for this neutralization reaction, it is possible to realize that one the neutralization products is water (pH=7) and the other one is the salt coming up from the cation of the NaOH and the anion of the HI:
Moreover, since the solubility of NaI is large in water, we infer it remains aqueous whereas the water is maintained as liquid:
Which is also balanced as the number of atoms of all the elements is the same at both sides.
Best regards!
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.
