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?
Indicate how to find the energy difference between two levels in cm-1, knowing that its value is 2.5x10-25 joules.
The gyromagnetic ratio (gamma) for 1H is 2.675x108 s-1 T-1. If the applied field is 1,409 T what will be the separation between nuclear energy levels?
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11. (10pts total) Consider the radical chlorination of 1,3-diethylcyclohexane depicted below. 4
• 6H total $4th total
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21 total
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a) (6pts) How many unique mono-chlorinated products can be formed and what are the
structures for the thermodynamically and statistically favored products?
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Number of Unique
Mono-Chlorinated Products
Thermodynamically
Favored Product
Statistically
Favored Product
b) (4pts) Draw the arrow pushing mechanism for the FIRST propagation step (p-1) for the
formation of the thermodynamically favored product. Only draw the p-1 step. You do
not need to include lone pairs of electrons. No enthalpy calculation necessary
H
H-Cl
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