There are cases for this answer..!!
SN1 will be faster if:
1.Reagent is weak base.
2.C connected to the Leaving Group is tertiary (sometimes
secondary) i.e. the leaving group must be a better
leaving group. the leaving ability is inversely proportional to
the bacisity of the compound (its basic character
3.The solvent used is polar protic (water and alcohols, etc.)
SN2 will be faster if:
1..Reagent is a strong base.
2.C connected to the LG is primary or a methyl group
(sometimes secondary)
3.The solvent used is polar aprotic (DMF, DMSO, etc.)
4. SN2 reactions need space to inter into the molecule and to
push the leaving group that’s why the molecule must not be
bulky.
Delivering a high-quality product at a reasonable price is not enough anymore.
That’s why we have developed 5 beneficial guarantees that will make your experience with our service enjoyable, easy, and safe.
You have to be 100% sure of the quality of your product to give a money-back guarantee. This describes us perfectly. Make sure that this guarantee is totally transparent.
Read moreEach paper is composed from scratch, according to your instructions. It is then checked by our plagiarism-detection software. There is no gap where plagiarism could squeeze in.
Read moreThanks to our free revisions, there is no way for you to be unsatisfied. We will work on your paper until you are completely happy with the result.
Read moreYour email is safe, as we store it according to international data protection rules. Your bank details are secure, as we use only reliable payment systems.
Read moreBy sending us your money, you buy the service we provide. Check out our terms and conditions if you prefer business talks to be laid out in official language.
Read more