Answer:
To synthesize cis-2-methylcyclopentyl from methycyclopentanol, you need to replace the acetate hydroxyl group with acetate by inverting the configuration.
Explanation:
To understand the process, you need to understand the nucleophilic mechanism taking place in the process. This is the first stage of the process. Hydroxide is a poor leaving group, to it must be converted to a good leaving group. To effect the change, it is necessary to use p-toluenesuphate.
p-toluenesuphate is favored because this can be prepared by a reaction that alters none of the bonds attached to the stereogenic center.
The reaction of p-toluensulfonate with potassium acetate in acetic acid effects the conversion to give the final product: cis-2-methylcyclopentyl.
Answer:
I think is A
Explanation: i'm not sure if im right.
Answer:
3
Explanation:
10.0 has 3 significant figures
<span>2AlPO4 ( aq) + 3MgCl2 (aq) -> Mg3(PO4)2 (s) + 2AlCl3 (aq) </span>
<span>Right answer is D
</span>
C! The clownfish hide in the sea anemones for protection
