Aspartame is an artificial sweetener marketed under the name Nutra-Sweet. A partial Lewis structure for aspartame is shown below. Aspartame can be classified as an organic compound (a compound based on carbon atoms). The majority of Lewis structures for simple organic compounds have all atoms with a formal charge of zero. Therefore, add lone pairs and multiple bonds to the structure above to give each atom a formal charge of zero when drawing the Lewis structure. Also note that the six-sided ring is shorthand notation for a benzene ring (—C 6 H 5 ). Benzene is discussed in Section 4-7. Complete the Lewis structure for aspartame. How many C and N atoms exhibit sp 1 hybridization? How many C and O atoms exhibit sp 3 hybridization? How many σ and π bonds are in aspartame?
Aspartame is an artificial sweetener marketed under the name Nutra-Sweet. A partial Lewis structure for aspartame is shown below. Aspartame can be classified as an organic compound (a compound based on carbon atoms). The majority of Lewis structures for simple organic compounds have all atoms with a formal charge of zero. Therefore, add lone pairs and multiple bonds to the structure above to give each atom a formal charge of zero when drawing the Lewis structure. Also note that the six-sided ring is shorthand notation for a benzene ring (—C 6 H 5 ). Benzene is discussed in Section 4-7. Complete the Lewis structure for aspartame. How many C and N atoms exhibit sp 1 hybridization? How many C and O atoms exhibit sp 3 hybridization? How many σ and π bonds are in aspartame?
Aspartame is an artificial sweetener marketed under the name Nutra-Sweet. A partial Lewis structure for aspartame is shown below.
Aspartame can be classified as an organic compound (a compound based on carbon atoms). The majority of Lewis structures for simple organic compounds have all atoms with a formal charge of zero. Therefore, add lone pairs and multiple bonds to the structure above to give each atom a formal charge of zero when drawing the Lewis structure. Also note that the six-sided ring is shorthand notation for a benzene ring (—C6H5). Benzene is discussed in Section 4-7. Complete the Lewis structure for aspartame. How many C and N atoms exhibit sp1 hybridization? How many C and O atoms exhibit sp3 hybridization? How many σ and π bonds are in aspartame?
Denote the dipole for the indicated bonds in the following molecules.
H3C
✓
CH3
B
F-CCl 3
Br-Cl
H3C Si(CH3)3
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OH
НО.
HO
HO
OH
vitamin C
CH3
For the SN2 reaction, draw the major organic product and select the correct (R) or (S) designation around the stereocenter
carbon in the organic substrate and organic product. Include wedge-and-dash bonds and draw hydrogen on a stereocenter.
Η
1
D
EN
Select Draw Templates More
C
H
D
N
Erase
Q9: Explain why compound I is protonated on O while compound II is protonated on N.
NH2
NH2
I
II
Chapter 4 Solutions
Bundle: Chemistry: An Atoms First Approach, 2nd, Loose-Leaf + OWLv2, 4 terms (24 months) Printed Access Card
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