Hot and spicy foods contain molecules that stimulate paindetecting nerve endings. Two such molecules are piperine and capsaicin: Piperine Capsaicin Piperine is the active compound in white and black pepper, and capsaicin is the active compound in chili peppers. The ring structures in piperine and capsaicin are shorthand notation. Each point where lines meet represents a carbon atom. a. Complete the Lewis structure for piperine and capsaicin, showing all lone pairs of electrons. b. How many carbon atoms ate sp , sp 2 , and sp 3 hybridized in each molecule? c. Which hybrid orbitals are used by the nitrogen atoms in each molecule? d. Give approximate values for the bond angles marked a through l in the above structures.
Hot and spicy foods contain molecules that stimulate paindetecting nerve endings. Two such molecules are piperine and capsaicin: Piperine Capsaicin Piperine is the active compound in white and black pepper, and capsaicin is the active compound in chili peppers. The ring structures in piperine and capsaicin are shorthand notation. Each point where lines meet represents a carbon atom. a. Complete the Lewis structure for piperine and capsaicin, showing all lone pairs of electrons. b. How many carbon atoms ate sp , sp 2 , and sp 3 hybridized in each molecule? c. Which hybrid orbitals are used by the nitrogen atoms in each molecule? d. Give approximate values for the bond angles marked a through l in the above structures.
Hot and spicy foods contain molecules that stimulate paindetecting nerve endings. Two such molecules are piperine and capsaicin:
Piperine
Capsaicin
Piperine is the active compound in white and black pepper, and capsaicin is the active compound in chili peppers. The ring structures in piperine and capsaicin are shorthand notation. Each point where lines meet represents a carbon atom.
a. Complete the Lewis structure for piperine and capsaicin, showing all lone pairs of electrons.
b. How many carbon atoms ate sp, sp2, and sp3 hybridized in each molecule?
c. Which hybrid orbitals are used by the nitrogen atoms in each molecule?
d. Give approximate values for the bond angles marked a through l in the above structures.
Diels Alder Cycloaddition: Focus on regiochemistry (problems E-F) –> match + of thedienophile and - of the diene while also considering stereochemistry (endo).
HELP! URGENT! PLEASE RESOND ASAP!
Question 4
Determine the rate order and rate constant for sucrose hydrolysis.
Time (hours)
[C6H12O6]
0
0.501
0.500
0.451
1.00
0.404
1.50
0.363
3.00
0.267
First-order, k = 0.210 hour 1
First-order, k = 0.0912 hour 1
O Second-order, k =
0.590 M1 hour 1
O Zero-order, k = 0.0770 M/hour
O Zero-order, k = 0.4896 M/hour
O Second-order, k = 1.93 M-1-hour 1
10 pts
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