Concept explainers
Interpretation:
To write the aldol condensation product of cyclohexanone.
Concept introduction:
Aldol reaction is a reversible reaction and occurs in the presence of a strong base like sodium hydroxide. One molecule (aldehyde or ketone) acts a nucleophile and attacks the electrophilic carbon center of the other molecule to give the addition product. The product is named
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Essential Organic Chemistry, Global Edition
- B-D-Glucose, a hemiacetal, can be converted to a mixture of acetals on treatment with CH,OH in the presence of acid. Draw a stepwise mechanism for this reaction. Explain why two acetals are formed from a single starting material. он он OH CH;OH, HCI HO Но HO HO но + Но + H20 OH OCH3 OH OHOCHS но B-D-glucosearrow_forwardDraw the keto form of the following enol.arrow_forward4) The following enone, 3-methylcyclopent-2-enone, was prepared through an intramolecular aldol condensation followed by a dehydration. Draw the starting diketone and the intermediate cyclic ß-hydroxy ketone. 3-methylcyclopent-2-enonearrow_forward
- Which of the following is the aldol addition product of two butanal molecules? O 2 CH3CH₂CH₂CH NaOH, H₂O 0° C 2-ethyl-3-hydroxyhexanal 2-methyl-2-hydroxyheptanal 3-ethyl-2-hydroxyhexanal 2-ethyl-2-hydroxyhexanalarrow_forward1.Does This have the ability to form a hemiacetal or acetal if acetone is added in the presence of heat and acid? Draw the product.arrow_forwardExplain why ketone K undergoes aldol reactions but ketone J does not.arrow_forward
- when an nitriles are treated with 1)NaOH,H2O/2)H3O+ , Explains what happens ?arrow_forwardWhich carbonyl groups in the anticancer drug Taxol will undergo nucleophilic addition, and which will undergo nucleophilic substitution?arrow_forwardShow how the following compounds can be synthesized from cyclohexanol.arrow_forward