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CH 3 Give correct IUPAC names for the following structures: 13 8. Он A& CI O2N. NO2 CI NO2llot o c. Bru 10 b. а...
5. Write the IUPAC names/ draw structures for the following: (10 points) a through f please...
5. Write the IUPAC names/ draw
structures for the following: (10 points)
a through f please
5. Write the IUPAC names/ draw structures for the following: (10 points) a. 2,4,6-trinitotoluene(TNT) b. O2N NH2 c. 2,6-dichloroanisole d. CI CHO COOH .
1)- Give the correct names for the structures drawn (i.e. A-E) or draw the structure for...
1)- Give the correct names for the structures drawn (i.e. A-E) or draw the structure for each of the names given (i.e., F) for the compounds below, and use the E/Z, cis/trans, equatorial/axial, R/S labeling when appropriate (Choose 4 overall which include A and E) он O2N NO2 CN NO2 Br Common Name (CH,)-СОНСОН(CH3)2 Common Name 4-Carbomethoxy-5-formyl-2-hydroxybenzenesulfonic acicd
1) Name the following carboxylic acids (use both IUPAC and common names): ОН ОН (b) (c)...
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...
1) Give the IUPAC Name the following Alkenes 3. Draw the structures to the following IUPAC names...
1) Give the IUPAC Name the following Alkenes
3. Draw the structures to the following IUPAC names:
2Methyl-1,5-hexadiene b- 1,3-dibromo-1,3-cyclohexadiene
а. ь. с.
а. ь. с.
1)- Give the correct names for the structures drawn (i.e. A-E) or draw the structure for each of the names given (i.e., F) for the compounds below, and use the E/Z, cis/trans, equatorial/axial, R/S l...
1)- Give the correct names for the structures drawn (i.e. A-E) or draw the structure for each of the names given (i.e., F) for the compounds below, and use the E/Z, cis/trans, equatorial/axial, R/S labeling when appropriate (Choose 4 overall which include A and E) он O2N NO2 CN NO2 Br Common Name (CH,)-СОНСОН(CH3)2 Common Name 4-Carbomethoxy-5-formyl-2-hydroxybenzenesulfonic acicd
1)- Give the correct names for the structures drawn (i.e. A-E) or draw the structure for each of the names given (i.e.,...
1. Give IUPAC names for the following compounds: O H.C =CH-C-NH2 H,00 H.CO 2. Draw structures...
1. Give IUPAC names for the following compounds: O H.C =CH-C-NH2 H,00 H.CO 2. Draw structures corresponding to each of the given names. Ethyl 4-aminobenzoate acetic formic anhydride 3. What is the order of decreasing reactivity towards nucleophilic acyl substitution for the carboxylic acid derivatives? (most reactive first) H,C-4-0--CHHC-2-N(CH) Hc--OCH, (CH),CH----OCH,
Give IUPAC names for the following structures. When appropriate, abbreviate ortho (o), meta (m), and para...
Give IUPAC names for the following structures. When appropriate, abbreviate ortho (o), meta (m), and para (p), no italics, if you elect to use these terms. он OCH3 CH3 ClI 1st structure: 2-methyltetrahydrofuran 2nd structure:
Provide the IUPAC names of the following compounds. (a) CH2CH2C=CCOOH (b) CH2CH(CH3)CHBCOOH (c) (CH3)2C=CHCOOH NO2 CH,...
Provide the IUPAC names of the following compounds. (a) CH2CH2C=CCOOH (b) CH2CH(CH3)CHBCOOH (c) (CH3)2C=CHCOOH NO2 CH, COOH d) COOH O, NVNO
Problem 8: Give IUPAC names for the compounds shown below. CI O CI Br کہللا کلید...
Problem 8: Give IUPAC names for the compounds shown below. CI O CI Br کہللا کلید مو CI 025 Q26 Q27 Problem 9: Provide reasonable starting materials for the following three compounds. Q28 Michael Acceptor Q29 Michael Donor 0= H Q30 Diene + Q31 Dienophile H Q32 SM1 + Q33 SM2
Give the IUPAC name for the following structures: Part II: Give the IUPAC name for each...
Give the IUPAC name for the following structures:
Part II: Give the IUPAC name for each of the following structures. (10 marks) 1. нс. CH CH3 CH3 2. нс. CH3 CH3 CH3 3 -CH3 CH3 CH3 4. F CH3 CI 5. À 6. HC CH3 Br CH3 H 7. H 8. H3C 9. HC CI HC CHE 10. H3c CH3
5. Write the IUPAC names/ draw
structures for the following: (10 points)
a through f please
5. Write the IUPAC names/ draw structures for the following: (10 points) a. 2,4,6-trinitotoluene(TNT) b. O2N NH2 c. 2,6-dichloroanisole d. CI CHO COOH .
1)- Give the correct names for the structures drawn (i.e. A-E) or draw the structure for each of the names given (i.e., F) for the compounds below, and use the E/Z, cis/trans, equatorial/axial, R/S labeling when appropriate (Choose 4 overall which include A and E) он O2N NO2 CN NO2 Br Common Name (CH,)-СОНСОН(CH3)2 Common Name 4-Carbomethoxy-5-formyl-2-hydroxybenzenesulfonic acicd
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...
1) Give the IUPAC Name the following Alkenes
3. Draw the structures to the following IUPAC names:
2Methyl-1,5-hexadiene b- 1,3-dibromo-1,3-cyclohexadiene
а. ь. с.
а. ь. с.
1)- Give the correct names for the structures drawn (i.e. A-E) or draw the structure for each of the names given (i.e., F) for the compounds below, and use the E/Z, cis/trans, equatorial/axial, R/S labeling when appropriate (Choose 4 overall which include A and E) он O2N NO2 CN NO2 Br Common Name (CH,)-СОНСОН(CH3)2 Common Name 4-Carbomethoxy-5-formyl-2-hydroxybenzenesulfonic acicd
1)- Give the correct names for the structures drawn (i.e. A-E) or draw the structure for each of the names given (i.e.,...
1. Give IUPAC names for the following compounds: O H.C =CH-C-NH2 H,00 H.CO 2. Draw structures corresponding to each of the given names. Ethyl 4-aminobenzoate acetic formic anhydride 3. What is the order of decreasing reactivity towards nucleophilic acyl substitution for the carboxylic acid derivatives? (most reactive first) H,C-4-0--CHHC-2-N(CH) Hc--OCH, (CH),CH----OCH,
Give IUPAC names for the following structures. When appropriate, abbreviate ortho (o), meta (m), and para (p), no italics, if you elect to use these terms. он OCH3 CH3 ClI 1st structure: 2-methyltetrahydrofuran 2nd structure:
Provide the IUPAC names of the following compounds. (a) CH2CH2C=CCOOH (b) CH2CH(CH3)CHBCOOH (c) (CH3)2C=CHCOOH NO2 CH, COOH d) COOH O, NVNO
Problem 8: Give IUPAC names for the compounds shown below. CI O CI Br کہللا کلید مو CI 025 Q26 Q27 Problem 9: Provide reasonable starting materials for the following three compounds. Q28 Michael Acceptor Q29 Michael Donor 0= H Q30 Diene + Q31 Dienophile H Q32 SM1 + Q33 SM2
Give the IUPAC name for the following structures:
Part II: Give the IUPAC name for each of the following structures. (10 marks) 1. нс. CH CH3 CH3 2. нс. CH3 CH3 CH3 3 -CH3 CH3 CH3 4. F CH3 CI 5. À 6. HC CH3 Br CH3 H 7. H 8. H3C 9. HC CI HC CHE 10. H3c CH3
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