Answer:
Four substitution products are obtained. The carbocation that forms can react with either nucleophile (H2O or CH3OH) from either the top or bottom side of the molecule
Explanation:
An SN1 reaction usually involves the formation of a carbocation in the slow rate determining step. This carbocation is now attacked by a nucleophile in a subsequent fast step to give the desired product.
However, the product is obtained as a racemic mixture because the nucleophile may attack from the top or bottom of the carbocation hence both attacks are equally probable.
The attacking nucleophile in this case may be water or CH3OH
Answer:
since there is a decimal point at the end, they are all significant figures so the answer is 5
Add 1 tsp. of vinegar to the canister at a time, filling it almost to the top. You need to add as much vinegar to the canister as possible without the vinegar and the baking soda coming into contact when you later snap the lid onto the canister. Depending on the exact canister, this may be around 5 tsp.
Haha i’m trying to do the same one i’ll make sure if i find out how too to get back to you!
