4. (22 points) "Fun in acid" question: Draw a reasonable mechanism using the curved-arrow formalism (include...
“Fun in acid” question: Draw a reaction mechanism using the curved-arrow formalism (include lone pair electrons) for the conversion of an ester into an alcohol and a methyl ester in the presence of acid in excess methanol. Hint: 6-steps.
“Fun in acid” question: Draw a reaction mechanism using the curved-arrow formalism (include lone pair electrons) for the following transesterification of an ester into an alcohol and a methyl ester in the presence of acid in excess methanol. Hint: 6-steps. H+
6. "Fun in base" question: Draw a reaction mechanism using the curved-arrow formalism (include lone pair electrons) for the conversion of methyl salicylate into the corresponding conjugate base of salicylic acid and methanol in the presence of excess aqueous hydroxide. Hint: The first step is an acid- base reaction. H20 осни + он o + CH OH (in excess; used as solvent) ОН Be sure you explain acid-base chemistry and use appropriate PK, values in steps 1 and 4. Compound...
QUESTION 1 Using the curved arrow formalism, outline an acceptable mechanism for the acid catalyzed electrophilic addition of water to 1-Methylcyclohexene as shown below. Your mechanism should show the movement of all electrons involved in bond forming and bond breaking steps as well as all formal charges for atoms that are not neutral CH, HO -H
Using the curved arrow formalism, outline an acceptable mechanism for the acid catalyzed electrophilic addition of water to 1-Methylcyclohexene as shown below. Your mechanism should show the movement of all electrons involved in bond forming and bond breaking steps as well as all formal charges for atoms that are not neutral. CH HOH H
Using the curved arrow formalism, outline an acceptable mechanism for the acid catalyzed electrophilic addition of water to 1-Methylcyclohexene as shown below. Your mechanism should show the movement of all electrons involved in bond forming and bond breaking steps as well as all formal charges for atoms that are not neutral CH, H-O-H H
Using the curved arrow formalism, outline an acceptable mechanism for the acid catalyzed electrophilic addition of water to 1-Methylcyclohexene as shown below. Your mechanism should show the movement of all electrons involved in bond forming and bond breaking steps as well as all formal charges for atoms that are not neutral. CH *** H-O-H H
Write a curved arrow mechanism for the acid catalyzed Fischer esterification of benzoic acid in CH3O*H (that is 0-18 labeled methanol). Show all steps, lone pair of electrons, charges and labeled O atoms through the mechanism.
please show work Using the curved arrow formalism, draw the mechanism for the reaction between N-acetyl-ptoluidine with concentrated nitric acid. Be sure to show all of the intermediates and rationalize the regioselectivity of the reaction.
Examine the curved arrow mechanism below, and answer the question in the box. If the mechanism is reasonable, draw all products. If the mechanism is not reasonable leave the drawing space blank. yes Is the curved arrow mechanism reasonable? no Н н сH,