The compound shown in the question is a cyclic hemiacetal.
When a hemiacetal is treated with aquous base a ketone is formed.
The detail mechanism is shown below.
to an aldehyde or ketone on 1. Provide a mechanism for the conversion of treatment with...
Acid-catalyzed hydration of an aldehyde or ketone is a reversible process. Provide the mechanism for how the hydrate is in equilibrium with the ketone below. Draw in all lone pairs, 1. curved arrows, and each proton transfer facilitated by solvent. но он Hао" Нао
12. Provide a curved arrow mechanism showing the conversion of the aldehyde to the cyclic ketal product. (6 pts)
12. Provide a curved arrow mechanism showing the conversion of the aldehyde to the cyclic ketal product. (6 pts) но: +Hy0 ное
12. Provide a curved arrow mechanism showing the conversion of the aldehyde to the cyclic ketal product. (6 pts) 10-M 13. Provide a synthesis for the target molecule shown. (18 pts) он TM SM он NC. SM TM
12. Provide a curved arrow mechanism showing the conversion of the aldehyde to the cyclic ketal product. (6 pts) Hot 13. Provide a synthesis for the target molecule shown. (18 pts) OH OH SM TM Oн NC. SM TM
10 12. Provide a eurved arrow mechanism showing the conversion of the aldehyde to the cyclic ketal product. (6 pts) ot sh 13. Provide a synthesis for the target molecule shown. (18 pts) SM TM Он NC SM TM
1. Draw the reactants and dehydrated aldol product for your assigned aldehyde–ketone pair. 2. Using your assigned aldehyde–ketone pair, draw a base-catalyzed mechanism producing the dehydrated aldol product, an α,β-unsaturated ketone. Aldehyde is benzaldehyde Ketone is cyclohexanone
OH to CH3 R R CEN сн. For reaction of an aldehyde or ketone to form a cyanohydrin (section 21.9 of the textbook), which of the following statements are true? Select all correct answers. The yield of this reaction is typically high. This can be carried out by reaction of "CN followed by aqueous workup (H*/H20). This can be carried out by reaction of the ketone with HCN. The product reverses back to starting materials upon treatment with base. The...
12. Provide a curved arrow mechanism showing the conversion of the aldehyde to the cyclic ketal product. (6 pts) 13. Provide a synthesis for the target molecule shown. (18 pts) NC OH SM CH TM SM Bonus: (10 pts) Starting from Benzene and using reagents that we have discussed in class, design a synthesis for the Target molecule (TM). HONHO
What is the aldol condensation product of cyclohexanone as the ketone and benzaldehyde as the aldehyde? Show the MECHANISM, REACTION, and provide NAME of product.