explain mechanistically how DMF catalyzed the formation of the acid chloride
explain mechanistically how DMF catalyzed the formation of the acid chloride
Explain mechanistically how DMF catalyzes the formation of the acid chloride (in the synthesis of N,N-Diethyl-m-toluamide)
Starting with a fatty acid located in the cytosol of the cell, explain “mechanistically” how a pantothenic acid deficiency may result in reduced acetyl CoA production from beta oxidation of palmitic acid.
Propose a mechanism for acid-catalyzed acetal formation
between propiophenone and ethylene glycol.
5. Propose a mechanism for acid-catalyzed acetal formation between propiophenone and ethylene glycol. (5 pts)
1. A common problem in the acid-catalyzed hydration of alkenes is the formation of an ether byproduct. Show the formation of the ether byproduct in relation to the reaction below by providing a curved-arrow mechanism for its formation. (2 pts) H307 Но + 0 OH
A cyanohydrins formation reaction of a ketone/aldchydc is often thought to be mechanistically analogous to base-catalysed hydration reaction. It is usually done in two steps. In the first step the ketone/aldehyde is mixed with a solution of sodium or potassium cyanide, which is followed by the addition of an acid, typically sulphuric acid. Please provide a mechanism for the following two-step procedure. (6') Can a cyanohydrin formation reaction occur at a reasonable rate under an acid-catalysed condition as shown below?...
Draw the reaction mechanism for the formation of hemiacetal and the acetal in the acid-catalyzed reaction of propanone with ethanol
Bonus: Draw a mechanism for the formation of the product in the acid-catalyzed reaction below. (0-5 pts) H-CI OH
complete the following reaction equations. explain product
formation and conditions.
он NaN3 ی بله DMF KOtBg Br
Show the reaction mechanism of the acid-catalyzed formation of this ester. Upload Choose a File DQuestion 6 2 pts Which of these is a tertiary amine? ?? OH
Explain the mechanism involved in the acid-catalyzed esterification of heptanoic acid with 1-butanol.