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12) Draw a line angle formula (you do not need to redraw f g, k, 1...
Due on February 6th at 9:00 am in 103 Williams, No Exceptions, No Excuses 1. Draw...
Due on February 6th at 9:00 am in 103 Williams, No Exceptions, No Excuses 1. Draw all the important resonance structures for the following ion showing all lone pairs of electrons, formal charges and double bonds. Show the electron flow by using arrows for full credit (6 points) For 1 bonus point label the resonance structure that is the most stable of the four below. 2. Fill in the boxes with the letter of the functional groups present in the...
Using the labels (A, B, C, etc.) from the list of functional groups provided, identify the...
Using the labels (A, B, C, etc.) from the list of functional
groups provided, identify the functional groups present in each of
the molecules on the next page. Some choices may be used more than
once, and some may not be used. Write your answers (letters only)
in the box under each compound. Use only these labels (i.e. if a
group appears that is not on the list, you do not need to include
it).
A) Alkyl halide
B) Ketone...
2. List the expected spectral data of 2-ethyl-3-hydroxy-hexanal observed from an IR, a 'H-NMR and mass...
2. List the expected spectral data of 2-ethyl-3-hydroxy-hexanal observed from an IR, a 'H-NMR and mass spectrum. CH3 -CH2 CH C-Hal C-N C-o CEC Intensity CEN Aromatic C=C C=0 220 200 180 160 140 120 60 40 20 0 ppm 100 80 Chemical shift (8) Intensity Bonding C-H Type of Vibration (Stretching unless noted) alkane CH -CH, alkene w-m m w-m bending bending out-of-plane bending alkyne arene Frequency (cm) 2850-3000 1375 and 1450 1450-1475 3000-3100 650-1000 3300 3030 690-900 2720...
Determine the enantiomeric excess (1) and indicate which configuration (2), S or R, is in excess....
Determine the enantiomeric excess (1) and indicate which configuration (2), S or R, is in excess. If R-3-bromo-2- methylhexane is -80 degrees, would a polarimetry reading of the mixture in this problem rotate light (3) clockwise (CW) or counterclockwise (CC) (8) Br Br 15% 85% (this question is worth 9 points, not 8 as stated in the picture) 1. determine enantiomeric excess (your answer should be a number) 2. determine whether excess is S or R. 3. Does the mixture...
____ 1. The diagram below represents serine, a polar, uncharged amino acid. Which functional group gives...
____ 1. The diagram below represents serine, a polar, uncharged
amino acid. Which functional group gives serine its
distinct property?
a. H3
b. CH2OH
c. –H
d. COO–
____ 2. The monomers shown below are monomers for which of the
following natural polymers?
a. polysaccharides
b. plastics
c. DNA
d. proteins
____ 3. Which of the following processes illustrates the production
of a protein?
a. specific code for amino acids --> amino acid chain -->
gene --> DNA --> specific...
26) Name the following compound. CH3 H2C=CH-CH2CHCH: A) 1,1-dimethyl-3-butane B) 4-methyl-1-pentene C) hexene D) 2-methyl-4-pentene E)...
26) Name the following compound. CH3 H2C=CH-CH2CHCH: A) 1,1-dimethyl-3-butane B) 4-methyl-1-pentene C) hexene D) 2-methyl-4-pentene E) 2-methylpentene 27) Name the following compound. CI A) 2,3,5-trichlorobenzene B) trichlorostyrene C) 1,3,4-trichlorobenzene D) 1,3,4-trichlorohexene E) 1,2,4-trichlorobenzene 28) Identify the formula for an alkene. A) CnH2n+4 B) CnH2n+2 C) CnH2n D) CnH2n-4 E) CnH2n-2 29) Name the following compound. A) 1,4-bromocyclohexene B) 1,4-dibromobenzene C) 3,6-dibromobenzene D) 2,5-dibromobenzene E) 2,5-dibromocyclohexene 30) Name the following compound. CECH CH,CH,CHCH A) 2-ethynebutane B) 3-methyl-1-pentyne C) 3-methyl-4-pentyne D) 3-ethyl-1-butyne...
Due on February 6th at 9:00 am in 103 Williams, No Exceptions, No Excuses 1. Draw all the important resonance structures for the following ion showing all lone pairs of electrons, formal charges and double bonds. Show the electron flow by using arrows for full credit (6 points) For 1 bonus point label the resonance structure that is the most stable of the four below. 2. Fill in the boxes with the letter of the functional groups present in the...
Using the labels (A, B, C, etc.) from the list of functional
groups provided, identify the functional groups present in each of
the molecules on the next page. Some choices may be used more than
once, and some may not be used. Write your answers (letters only)
in the box under each compound. Use only these labels (i.e. if a
group appears that is not on the list, you do not need to include
it).
A) Alkyl halide
B) Ketone...
2. List the expected spectral data of 2-ethyl-3-hydroxy-hexanal observed from an IR, a 'H-NMR and mass spectrum. CH3 -CH2 CH C-Hal C-N C-o CEC Intensity CEN Aromatic C=C C=0 220 200 180 160 140 120 60 40 20 0 ppm 100 80 Chemical shift (8) Intensity Bonding C-H Type of Vibration (Stretching unless noted) alkane CH -CH, alkene w-m m w-m bending bending out-of-plane bending alkyne arene Frequency (cm) 2850-3000 1375 and 1450 1450-1475 3000-3100 650-1000 3300 3030 690-900 2720...
Determine the enantiomeric excess (1) and indicate which configuration (2), S or R, is in excess. If R-3-bromo-2- methylhexane is -80 degrees, would a polarimetry reading of the mixture in this problem rotate light (3) clockwise (CW) or counterclockwise (CC) (8) Br Br 15% 85% (this question is worth 9 points, not 8 as stated in the picture) 1. determine enantiomeric excess (your answer should be a number) 2. determine whether excess is S or R. 3. Does the mixture...
____ 1. The diagram below represents serine, a polar, uncharged
amino acid. Which functional group gives serine its
distinct property?
a. H3
b. CH2OH
c. –H
d. COO–
____ 2. The monomers shown below are monomers for which of the
following natural polymers?
a. polysaccharides
b. plastics
c. DNA
d. proteins
____ 3. Which of the following processes illustrates the production
of a protein?
a. specific code for amino acids --> amino acid chain -->
gene --> DNA --> specific...
26) Name the following compound. CH3 H2C=CH-CH2CHCH: A) 1,1-dimethyl-3-butane B) 4-methyl-1-pentene C) hexene D) 2-methyl-4-pentene E) 2-methylpentene 27) Name the following compound. CI A) 2,3,5-trichlorobenzene B) trichlorostyrene C) 1,3,4-trichlorobenzene D) 1,3,4-trichlorohexene E) 1,2,4-trichlorobenzene 28) Identify the formula for an alkene. A) CnH2n+4 B) CnH2n+2 C) CnH2n D) CnH2n-4 E) CnH2n-2 29) Name the following compound. A) 1,4-bromocyclohexene B) 1,4-dibromobenzene C) 3,6-dibromobenzene D) 2,5-dibromobenzene E) 2,5-dibromocyclohexene 30) Name the following compound. CECH CH,CH,CHCH A) 2-ethynebutane B) 3-methyl-1-pentyne C) 3-methyl-4-pentyne D) 3-ethyl-1-butyne...
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