Answer:
Explanation:
In organic chemistry, the reaction between 2-butanol with TsCl and Et3N is known as the tosylation of the alcohol hydroxyl group. Alcohol is being changed to tosylate by the use of tosyl chloride under the influence of a base. Tosylation of alcohol is an example of a nucleophilic substitution reaction. From the image attached below, we will see how the reaction between 2-butanol proceed into the product by using tosyl chloride and a base(Et3N).
Answer:
Explanation:
Structure of the 2,2,4,4-tetramethyl-3-pentanone is give in the attachment
In 2,2,4,4-tetramethyl-3-pentanone, no alpha hydrogen is present, therefore, enol form is not possible and hence, exist only in keto form.
Explanation for existence of cyclohexa-2,4-diene-1-one only in enol form:
keto form of cyclohexa-2,4-diene-1-one not aromatic and hence less stable.
Whereas enol form it is aromatic which makes it highly stable. that's why cyclohexa-2,4-diene-1-one exists only in enol form.
