7. The reaction is: он a) This reaction involves four organic molecules. Label the structures with their names. b)...
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
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,...
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
Identify the functional groups in the following molecules (Use names from the table below List cach class of functional group only once, If there are fewer than 3 functional groups, leave an appropriate number of answer hoxes ampty) COH NHs b) HC CHi Structures of Some Common Punctional Ciroups Name Stracture Name Stracture 2u Alkene Nitro Allkyne Thiol Arene Aldebyd Halsde Koson r.CLO Caroxyli Acid Alohol Ester Elher Ade Amin Earbocyl id Nitrila
The terminal structures of the three common blood group antigens are shown below.' но он но Чоно -OH 10 но Но он HO - ОН HO HONOR -OR он і но но но A Antigen B Antigen H(O) Antigen 1. (4 points) Circle the glycosidic bonds present in the A antigen and name them using alpha/beta designations and numbers - no sugar names.
Review Topics Reference Identify the functional groups in the following molecules. Use names from the table below. Listeach class of functional group only once. If there are fewer than 3 functional groups, leave an appropriate number of answer boxes at H.N. CH, amine Structures of Some Common Functional Groups Structure Same Structure Same Alkene Nitro Thiel
1) Name the following carboxylic acids (use both IUPAC and common names): ОН ОН (b) (c) ОН ОН (d) Br ОН ОН NH2 2) Draw the condensed and line structures for the following compounds (a) 3,4-dimethylhexanoic acid (b) Phenylacetic acid (c) 3,4-dinitrobenzoic acid (d) 2,2,3-triflurobutanoic acid (e) 3-hydroxybutanoic acid (1) o-hydroxybenzoic acid (g) a-aminopropionic acid 3) Name the following dicarboxylic acids (use both IUPAC and common names) Он (а) НО ОН НО. (b) он ОН ОН (d) ОН он ОН...
juri seaniay write any Review Topics Relerences] req 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, leave an appropriate number of answer boxes empty) Visited но chrysanthemic acid 2req 2req b) epibatadine, analgesic from skin of neotropical frog, 200x potency of morphine Structures of Some Common Functional Groups Name Structure Name Structure Alkene Nitro SH -CC- Alkyne Thiol...
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
Organic Chemistry 1. Draw each one of the following molecules and label it as: alkyl halide, allyl halide or vinyl halide a) 2-chloro-3-ethylpentane b) 6-ethyl-3-lodocyclohexene 2. Give all resonance structures of the allylic radical intermediate that arise from reaction above. All allylic C-H on the molecule are equivalent so only show the two resonance structures arising from one C-H bond reacting. 3. Are the resonance structures above equivalent or non-equivalent? 4. Give all the products expected from the reaction above....