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7) label the functional Molecules below groups on the no la w wampon 3) Honeyde Dahil...
Circle and label the functional groups in the molecules below: Circle and label the functional groups...
Circle and label the functional groups in the molecules below:
Circle and label the functional groups in the molecules below:
answer (3 pts) 4 of 6 7. Label all functional groups present within the following molecules....
answer (3 pts) 4 of 6 7. Label all functional groups present within the following molecules. Ifa higher priority functional group is comprised of two or more other functional groups, label the higher priority group only. (2 pts each) OH penicillin 8. Which of the following compounds is/are optically active? Circle your answer. (2 pts each) meso-tartaric acid L-cysteine 1.4-butanediol (R)-2-iodohexane 9. Rank the following in order of increasing acidity. (5 pts) HF CH3NH2 CH3OH HB CH3CH2CH2CH2CH3
7. Label all functional groups present within the following molecules. If a higher priority functional group...
7. Label all functional groups present within the following molecules. If a higher priority functional group is comprised of two or more other functional groups, label the higher priority group only. (2 pts each) он penicillin G 8. Which of the following compounds is/are optically active? Circle your answer. (2 pts each) meso-tartaric acid L-cysteine 1,4-butanediol (R)-2-iodohexane 9. Rank the following in order of increasing acidity. (5 pts) СH3NH2 снзон HBr СHЗCH2CH2CH2СH3 HF
7. Label all functional groups present within the following molecules. If a higher priority functional group...
7. Label all functional groups present within the following molecules. If a higher priority functional group is comprised of two or more other functional groups, label the higher priority group only. (2 pts each) OH penicillin G 8. Which of the following compounds is/are optically active? Circle your answer. (2 pts each) meso-tartaric acid L-cysteine 1,4-butanediol (R)-2-iodohexane 9. Rank the following in order of increasing acidity. (5 pts) HF CH3NH2 CH3OH HBr CH3CH2CH2CH2CH3
Identify functional groups of the above molecules using the table given. Identify the functional groups in the following...
Identify functional groups of
the above molecules using the table given.
Identify the functional groups in the following molecules. (Use names from the table below. List each class of functional group only once. If there are fewer than 3 functional groups, lcave an appropriate number of answer boxes empty.) OH а) NH2 phenylalanine Cн-он b) NHCH Structures of Some Common Functional Groups Name Structure Name Structure X Alkene Nitro Alkyne C C Thiol Aldehyde Arene Halide Ketone (XF, CI, Br,...
3) Circle and the functional groups in the following molecules: (6 pts.) a) Capsaicin: (compound responsible...
3) Circle and the functional groups in the following molecules: (6 pts.) a) Capsaicin: (compound responsible for burning sensation of hot sauce) gagne b) Amoxicillin: (Anti-biotic effective against many bacteria) NH2 но- 4) Draw the enantiomer of the following molecules: (3 pts) NH2 Tyrosine
Label the boxed functional groups in the steroid molecule. 1) 2) 3) Label the boxed functional...
Label the boxed functional groups in the steroid molecule.
1)
2)
3)
Label the boxed functional groups in the steroid molecule. In each reaction box, place the best reagent and conditions from the list below. In each reaction box, place the best reagent and conditions from the list below.
What are the functional groups of the molecules drawn below? CH3CH2CH2CH2CH CH3CH2CCH2CHCH2CH3 CH3 HzCY NH2 OH...
What are the functional groups of the molecules drawn
below?
CH3CH2CH2CH2CH CH3CH2CCH2CHCH2CH3 CH3 HzCY NH2 OH d) – (This molecule has 2. One of them is NOT an amide...why?) and
Label the functional groups below in the infrared spectrum of acetone.
Label the functional groups below in the infrared spectrum of acetone.
WH83 SU 7. Recognizing functional groups: Circle each functional group and then label each group with...
WH83 SU 7. Recognizing functional groups: Circle each functional group and then label each group with the name of the group. NH OH COOH Alcohols | Chemistry 1113 87
WH83 SU 7. Recognizing functional groups: Circle each functional group and then label each group with the name of the group. NH OH COOH Alcohols | Chemistry 1113 87
Circle and label the functional groups in the molecules below:
Circle and label the functional groups in the molecules below:
answer (3 pts) 4 of 6 7. Label all functional groups present within the following molecules. Ifa higher priority functional group is comprised of two or more other functional groups, label the higher priority group only. (2 pts each) OH penicillin 8. Which of the following compounds is/are optically active? Circle your answer. (2 pts each) meso-tartaric acid L-cysteine 1.4-butanediol (R)-2-iodohexane 9. Rank the following in order of increasing acidity. (5 pts) HF CH3NH2 CH3OH HB CH3CH2CH2CH2CH3
7. Label all functional groups present within the following molecules. If a higher priority functional group is comprised of two or more other functional groups, label the higher priority group only. (2 pts each) он penicillin G 8. Which of the following compounds is/are optically active? Circle your answer. (2 pts each) meso-tartaric acid L-cysteine 1,4-butanediol (R)-2-iodohexane 9. Rank the following in order of increasing acidity. (5 pts) СH3NH2 снзон HBr СHЗCH2CH2CH2СH3 HF
7. Label all functional groups present within the following molecules. If a higher priority functional group is comprised of two or more other functional groups, label the higher priority group only. (2 pts each) OH penicillin G 8. Which of the following compounds is/are optically active? Circle your answer. (2 pts each) meso-tartaric acid L-cysteine 1,4-butanediol (R)-2-iodohexane 9. Rank the following in order of increasing acidity. (5 pts) HF CH3NH2 CH3OH HBr CH3CH2CH2CH2CH3
Identify functional groups of
the above molecules using the table given.
Identify the functional groups in the following molecules. (Use names from the table below. List each class of functional group only once. If there are fewer than 3 functional groups, lcave an appropriate number of answer boxes empty.) OH а) NH2 phenylalanine Cн-он b) NHCH Structures of Some Common Functional Groups Name Structure Name Structure X Alkene Nitro Alkyne C C Thiol Aldehyde Arene Halide Ketone (XF, CI, Br,...
3) Circle and the functional groups in the following molecules: (6 pts.) a) Capsaicin: (compound responsible for burning sensation of hot sauce) gagne b) Amoxicillin: (Anti-biotic effective against many bacteria) NH2 но- 4) Draw the enantiomer of the following molecules: (3 pts) NH2 Tyrosine
Label the boxed functional groups in the steroid molecule.
1)
2)
3)
Label the boxed functional groups in the steroid molecule. In each reaction box, place the best reagent and conditions from the list below. In each reaction box, place the best reagent and conditions from the list below.
What are the functional groups of the molecules drawn
below?
CH3CH2CH2CH2CH CH3CH2CCH2CHCH2CH3 CH3 HzCY NH2 OH d) – (This molecule has 2. One of them is NOT an amide...why?) and
Label the functional groups below in the infrared spectrum of acetone.
WH83 SU 7. Recognizing functional groups: Circle each functional group and then label each group with the name of the group. NH OH COOH Alcohols | Chemistry 1113 87
WH83 SU 7. Recognizing functional groups: Circle each functional group and then label each group with the name of the group. NH OH COOH Alcohols | Chemistry 1113 87
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