draw the mechanism for both Н+ a) он он Hacid catalyzed ОН- b) OH он H...
Draw the mechanism for the following reaction
НО НО ОН НО ОН НО. Н. [H+] EAS [н'] EAS
These monosaccharides are
CH,OH CH,OH H ОН НО НО H ОНОН Н. ОН 1 Н НО Н. H Н H H H ОН.
3) Which of the following compounds is chiral? A) H Н-С-н н B) H HO C-OH Н C) CH3 HO-C-H Cl D) Br Н-С-ОН н E) C Br- C-C Br 4) In the L- isomer of a Fischer projection of a monosaccharide, the -OH group furthest from the carbonyl is written A) on the left of the top chiral carbon B) on the right of the top chiral carbon C) on the left of the middle chiral carbon D) on...
How do I draw the mechanism?
OCH3 OCH3 Н+ ОН Он
Select the product for the following reaction: HO+H нон нон н +он CH,OH он ноо нонно он нон HO+H нон н+он н+он нон н он н +он нон нон н-он нон нон CH OH сн,он CH OH CH,OH 4 оооо
Draw the mechanism for both reactions. The top reaction is Base
Catalyzed Ester Hydrolysis and the bottom is Addition/Elimination
Ester and Amide Mechanisms.
H2O HOR HO 0 H,09
below) но HO он но Isomer A Isomer B (2 points) Propose a reasonable base catalyzed mechanism (use OH as the base catalyst) for the conversion of Isomer A to Isomer B How many different types of H are in isomer A? How many different types of H are in isomer B?
helppp
Reaction B Select Draw Rings More Erase O = G reduction н—сон H-C-OH HC-OH UU H- нс — он
Be sure to answer all parts Draw a stepwise mechanism for the conversion of pentan-3-one to its enol form: ОН H,о Н-0 Part 1: НО н О2 Н-о* view structure view structure Н-0 Part 2 out of 3 он edit structure... edit structure...
20) Which compound would be most acidic? a) HO b) ОН OH e) н H