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:The molar mass of a compound cab be find by adding up all the molar mass of the element present in the compound... Check the image for more clarification
Explanation:
Answer:
[Ne] 2s2 2p3
Explanation:
Phosphorus will most likely have an ion that will be 3- because it wants to have a full outer shell. Thus, the elctron configuration is: 1s2 2s2 2p6 3s2 3p3.
Not elementary school work
Answer:
Precent yield
Explanation:
This is takes into account how much of a substance should have been created (theoretical yield) and compares it to what was actually created (the actual yield).
