Answer:
Explanation:
The stereochemical structures of the two compounds of the fumarase-catalyzed reaction are in the attachment below. The reaction been referred to is illustrated in the equation below
HOOCCH=CHCOOH + H₂O ==> HOOCCH₂CH(OH)COOH
The compounds attached are trans-2-butenedioate (which is one of the reactants) and (s)-2-hydroxysuccinate (which is the product formed)
Note that stereoisomers are isomers that differ in spatial orientation, thus there are other isomers that could contain the same atoms and have slightly but different spatial orientation such as cis-2-butenedioate and (r)-2-hydroxysuccinate
Answer:
9-10 ppm.
0.2-0.4 ppm.
Explanation:
The proton on the aldehyde group will appear at approximately 9-10 ppm whereas the methylene peak on the alcohol is the only peak 0.2-0.4 ppm for either compound. Aldehydes and aromatics are quite distinctive in the Nuclear magnetic resonance (NMR). Aldehydes show up from 9-10 ppm, usually as a small singlet; aromatic protons show up from 6.5-8.5 ppm. NMR spectroscopy is the use of NMR to study the physical, chemical, and biological properties of matter.
Answer:
B is the correct answer.
......Hopefully it it helpful.......
#1 is 6
#2 During chemistry lab, Mrs. Black’s students placed an antacid tablet in a zip lock bag. They recorded the mass of the tablet in the bag. Then they carefully added 50 grams of water and quickly sealed the bag. The tablet began to fizz and soon disappeared. The bag was filled with gas and it felt cold to the touch.