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WH83 SU 7. Recognizing functional groups: Circle each functional group and then label each group with...
1. Identify all the functional groups in the following compounds. Circle each functional group and label...
1. Identify all the functional groups in the following
compounds. Circle each functional group and label each group.
Thank you!
1. Identify all the functional groups in the following compounds. Circle each functional group and label each group. Hiç O CH CH CH-C-0-CHCH, -0-CH, CH CH(CH), a. acid group СОН) -CH-CHNHA 0-C-CH Amphetamine (a central nervous system stimulant and abused drug) O Aspirin ( 13 H1802 . . HC=CHCHACHACHCH CHO CHE e. HCCHI (CH OH CHE Citronellal alcohol group ~...
1) Label the acidic functional groups 2) For each acidic site, indicate if it has been...
1) Label the acidic functional groups
2) For each acidic site, indicate if it has been drawn in the
protonated form or not
9/1/16 Name: Worksheet 2 Below is a partial structure of Humic Acid, Circle AND name SEVEN different functional groups on the molecule НООС HOOC сно нс-он COOH --0 он НО. но-сн НО он ( ОН нс-он COOH о HC-OH с=0 o- НО но оноо ОН HN NH
Circle and label all functional groups in Aldosterone and Oxandrolone. Be sure to label any alcohols...
Circle and label all functional groups in Aldosterone and Oxandrolone. Be sure to label any alcohols as primary, secondary, or tertiary. Additionally, label one quaternary carbon in each molecule. OH OH HO Oxandrolone Aldosterone
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
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:
Q1. Circle all functional groups (if any) and name them. Put the functional group of the...
Q1. Circle all functional groups (if any) and name them. Put the functional group of the highest priority in the box. That group will determine the name of a compound 02. Name the compounds from above Q3. Practice the amines and amide nomenclature (not discussed in class for the following compounds: Amines NH NH2 Amides: H2N
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
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
1. For the molecule below a) Circle and label all functional groups. b) Name all intermolecular...
1. For the molecule below a) Circle and label all functional groups. b) Name all intermolecular forces present in the molecule: Amane Aromates hetone lendon dspervon Dipale -Dipole Amine Aromatr 2. For the molecule below a) Box in all atoms that can hydrogen bond with water but not with acetone (CH3OCHS) b) Label all electrophilic carbons (use 6*) NH c) Label the least basic nitrogen. НО d) Label the most acidic hydrogen
1. In each molecule A-F below, circle and name two functional groups/moieties present in the molecule....
1. In each molecule A-F below, circle and name two functional groups/moieties present in the molecule. Select from the list provided. [alcohol, ether, aldehyde, carboxylic acid, ester, amine, amide, propyl, alkyne, alkene - label as cis or trans when applicable, arene (for aromatic group)]. H2N- CH-OH CH2 HO H2CO | 0 NHA H2N IZ HO I- 0 m
1. Identify all the functional groups in the following
compounds. Circle each functional group and label each group.
Thank you!
1. Identify all the functional groups in the following compounds. Circle each functional group and label each group. Hiç O CH CH CH-C-0-CHCH, -0-CH, CH CH(CH), a. acid group СОН) -CH-CHNHA 0-C-CH Amphetamine (a central nervous system stimulant and abused drug) O Aspirin ( 13 H1802 . . HC=CHCHACHACHCH CHO CHE e. HCCHI (CH OH CHE Citronellal alcohol group ~...
1) Label the acidic functional groups
2) For each acidic site, indicate if it has been drawn in the
protonated form or not
9/1/16 Name: Worksheet 2 Below is a partial structure of Humic Acid, Circle AND name SEVEN different functional groups on the molecule НООС HOOC сно нс-он COOH --0 он НО. но-сн НО он ( ОН нс-он COOH о HC-OH с=0 o- НО но оноо ОН HN NH
Circle and label all functional groups in Aldosterone and Oxandrolone. Be sure to label any alcohols as primary, secondary, or tertiary. Additionally, label one quaternary carbon in each molecule. OH OH HO Oxandrolone Aldosterone
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
Circle and label the functional groups in the molecules below:
Circle and label the functional groups in the molecules below:
Q1. Circle all functional groups (if any) and name them. Put the functional group of the highest priority in the box. That group will determine the name of a compound 02. Name the compounds from above Q3. Practice the amines and amide nomenclature (not discussed in class for the following compounds: Amines NH NH2 Amides: H2N
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
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
1. For the molecule below a) Circle and label all functional groups. b) Name all intermolecular forces present in the molecule: Amane Aromates hetone lendon dspervon Dipale -Dipole Amine Aromatr 2. For the molecule below a) Box in all atoms that can hydrogen bond with water but not with acetone (CH3OCHS) b) Label all electrophilic carbons (use 6*) NH c) Label the least basic nitrogen. НО d) Label the most acidic hydrogen
1. In each molecule A-F below, circle and name two functional groups/moieties present in the molecule. Select from the list provided. [alcohol, ether, aldehyde, carboxylic acid, ester, amine, amide, propyl, alkyne, alkene - label as cis or trans when applicable, arene (for aromatic group)]. H2N- CH-OH CH2 HO H2CO | 0 NHA H2N IZ HO I- 0 m
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