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1. Name the following compounds: b. C. Cl Cl он 2. Draw the following compounds: a....
ctions 5. Fill in the ising bonconllg L Hg-CM-Ch c-c-ch3 2. Draw structures for the following...
ctions 5. Fill in the ising bonconllg L Hg-CM-Ch c-c-ch3 2. Draw structures for the following compounds. a) 2-vinyl-1,3-cyclohexadiene b) 4-methyl-2-pentene. c) octa-2,4-diene d) deca-1,5-diene e) 3-heptene f 4-methyl-2-pentene 9) trans-8-ethyl-3-undecen h) E-5-bromo-4-chloro-7,7-dimethyl-4-undecene D Z-1,2-difluoro-cyclohexene )4-ethenylcyclohexano 1. Predict the major organic product or products of each of the following reactions. H2SO a) (CH)2CHCH-CH2 н.о 1. Hg(OAc)2, H2O b) (CH),CHCH-СH, 2. NaBH 1. BH3-THF c) (CH),СHCH-CH, 2. H2O2, NaOH
for f - j draw structures pls help with #1 as well f) 4-methyl-2-pentene 9) trans-8-ethyl-3-undecen...
for f - j draw structures pls help with #1 as well
f) 4-methyl-2-pentene 9) trans-8-ethyl-3-undecen h) E-5-bromo-4-chloro-7,7-dimethyl-4-undecene i) Z-1,2-difluoro-cyclohexene i) 4-ethenylcyclohexano Predict the major organic product or products of each of the following reactions. a) (CH3),CHCH-CH: H2SO4 HO b) (CH3),CHCH-CH, 1. Hg(OAc), H20 2. NaBH4 1. BH-THF c) (CH3),CHCH-CH2 2. H,O, NaOH
1) Draw structures for compounds named below. A) (Z)-1-bromo-2-chloro-1-heptene B) 4-chloro-4-fluoro-2-octyne
1) Draw structures for compounds named below. A) (Z)-1-bromo-2-chloro-1-heptene B) 4-chloro-4-fluoro-2-octyne
1. 3-methyl-1-butene on reaction with H-Cl forms two products, namely 2-chloro-3- methylbutane (minor) and 2-chloro-2-methylbutane (major)....
1. 3-methyl-1-butene on reaction with H-Cl forms two products, namely 2-chloro-3- methylbutane (minor) and 2-chloro-2-methylbutane (major). Illustrate the mechanism for the formation of these two products. Use curved arrows to illustrate electron movement and all intermediates must be shown. 2. 3,3-dimethyl-1-butene on reaction with HBr forms two products, namely 3-bromo-2,2- dimethylbutane (minor) and 2-bromo-2,3-dimethylbutane (major). Illustrate the mechanism for the formation of these two products. Use curved arrows to illustrate electron movement and all intermediates must be shown. 3. Calculate...
1. Name the following compounds properly, including stereochemistry a) b) CHs Cl NO NH2 2. Draw...
1. Name the following compounds properly, including stereochemistry a) b) CHs Cl NO NH2 2. Draw the structures of the following compounds. 16 a) o-bromophenol d) trans 1,4-diphenyl-2-butene b) 3.4-dinitrobenzaldehyde c) p-isopropylbenzoic acid 3. a) Draw an example of a CoHio compound with conjugated double bonds /2 of an aromatic cation. c) Draw an example of an aromatic anion. 5 4. Circle all of the following which are aromatic. co
C trans-3-Methyl-2-pentru agen.wileyplus.com/edugen/student/mainfr.uni Klein, Organic Chemistry, 3e CO7T1002478 Give an IUPAC name for the following compound:...
C trans-3-Methyl-2-pentru agen.wileyplus.com/edugen/student/mainfr.uni Klein, Organic Chemistry, 3e CO7T1002478 Give an IUPAC name for the following compound: cycloheptene cyclohexene dy cyclopropene cyclobutene cyclopentene * C trans-3-Methyl-2-pentene C6H gen.wileyplus.com/edugen/student/mainfr.uni JS Klein, Organic Chemistry, 3e CO7T1007433 Which of the following structures could be considered a 4-methyl-1-pentene? LUS Klein, Organic Chemistry, 3e ECES CO7T1002771 Which of the following structures could be considered a 3-heptene? study LUS Klein, Organic Chemistry, 3e RCES COZT10Q2850 Give an IUPAC name for the following compound: (E)-4-hexene (Z)-3-heptene (E)-2-heptene (Z)-4-heptene...
1) Draw structures for compounds named below. A) (2)-1-bromo-2-chloro-1-heptene B) 4-chloro-4-fluoro-2-octyne 2) Gi...
1) Draw structures for compounds named below. A) (2)-1-bromo-2-chloro-1-heptene B) 4-chloro-4-fluoro-2-octyne 2) Give IUPAC name for the following structure. 3) For each reaction below, indicate which starting material is the Nucleophile and which is the Electrophile. Show arrows to demonstrate how the transformation occurs. →^_^tts a Porto ~ onde gi 4) Draw a mechanism for the conversion of the shown starting material to the corresponding product. 5) In the transformation below, a starting material is treated with HCl to form...
lculate the degrees of unsaturation in the following compounds. a. C12H16N302Br b. C8H10C14 c. C9H20N4 d....
lculate the degrees of unsaturation in the following compounds. a. C12H16N302Br b. C8H10C14 c. C9H20N4 d. C15H18 4. Draw structures for the following hydrocarbons. a. 3,5-diethyl-4-isopropyl-2,6-octadiene b. 4,5-dimethyl-1,4,7-decatriene c. 1-chloro-3-bromo-3-heptene d. 2-methyl-1,3-cyclopentadiene e. 4-isopropylcyclohexene
Name or draw the following Prepare the following using reagents or conditions necessary. Name: CHM 2210...
Name or draw the following
Prepare the following using reagents or conditions
necessary.
Name: CHM 2210 Exam 1 Fall 2019 1. Name or draw the following (3 pts each, 18 pts) a. Trans-1,3-Difluorocyclopentane b. (Z)-5-Ethyl-4-isopropyl-1,5-heptadiene c. (3,5E,7Z)-5,7-Diethyl-4-methyl-3,5,7-decatriene that - - hexene d. propyl 2- Bromo-4 propyl t-hexene 3.5-octadiene E e. $23-chloro-6-methyl-3.5-octadiene Me e 3-Ethyl-2-methyl-4-nitro-l-nonene ON nitro ОН Br Br - он All/Br Markou КОН - H₂O H3Rou 2sche + ALI ОН ОН ВСоон BH3 THE ноо оң Arcool-1
JI) Name the compounds or draw the structures from their names. (2 pts) 1,2-chovo mul COOH...
JI) Name the compounds or draw the structures from their names. (2 pts) 1,2-chovo mul COOH a) NO2 b) CI c) 4-phenyl-2-pentanol; •DH d) 1-bromo-2-chloro-4-ethylbenzene; 2. Arrange the compounds in each set in order of decreasing reactivity (fastest to slowest) toward EAS. Explain. (2 pts) 0-C-CH3 -C-0-CH3 a) (A) (B) (C) CH2CH3 -NH2 ( C1) do nosotros (B) b) (A) 3. Account for the observation that trifluoromethyl groups is meta directing, as shown in the following example. (1 pt) CF3...
ctions 5. Fill in the ising bonconllg L Hg-CM-Ch c-c-ch3 2. Draw structures for the following compounds. a) 2-vinyl-1,3-cyclohexadiene b) 4-methyl-2-pentene. c) octa-2,4-diene d) deca-1,5-diene e) 3-heptene f 4-methyl-2-pentene 9) trans-8-ethyl-3-undecen h) E-5-bromo-4-chloro-7,7-dimethyl-4-undecene D Z-1,2-difluoro-cyclohexene )4-ethenylcyclohexano 1. Predict the major organic product or products of each of the following reactions. H2SO a) (CH)2CHCH-CH2 н.о 1. Hg(OAc)2, H2O b) (CH),CHCH-СH, 2. NaBH 1. BH3-THF c) (CH),СHCH-CH, 2. H2O2, NaOH
for f - j draw structures pls help with #1 as well
f) 4-methyl-2-pentene 9) trans-8-ethyl-3-undecen h) E-5-bromo-4-chloro-7,7-dimethyl-4-undecene i) Z-1,2-difluoro-cyclohexene i) 4-ethenylcyclohexano Predict the major organic product or products of each of the following reactions. a) (CH3),CHCH-CH: H2SO4 HO b) (CH3),CHCH-CH, 1. Hg(OAc), H20 2. NaBH4 1. BH-THF c) (CH3),CHCH-CH2 2. H,O, NaOH
1) Draw structures for compounds named below. A) (Z)-1-bromo-2-chloro-1-heptene B) 4-chloro-4-fluoro-2-octyne
1. 3-methyl-1-butene on reaction with H-Cl forms two products, namely 2-chloro-3- methylbutane (minor) and 2-chloro-2-methylbutane (major). Illustrate the mechanism for the formation of these two products. Use curved arrows to illustrate electron movement and all intermediates must be shown. 2. 3,3-dimethyl-1-butene on reaction with HBr forms two products, namely 3-bromo-2,2- dimethylbutane (minor) and 2-bromo-2,3-dimethylbutane (major). Illustrate the mechanism for the formation of these two products. Use curved arrows to illustrate electron movement and all intermediates must be shown. 3. Calculate...
1. Name the following compounds properly, including stereochemistry a) b) CHs Cl NO NH2 2. Draw the structures of the following compounds. 16 a) o-bromophenol d) trans 1,4-diphenyl-2-butene b) 3.4-dinitrobenzaldehyde c) p-isopropylbenzoic acid 3. a) Draw an example of a CoHio compound with conjugated double bonds /2 of an aromatic cation. c) Draw an example of an aromatic anion. 5 4. Circle all of the following which are aromatic. co
C trans-3-Methyl-2-pentru agen.wileyplus.com/edugen/student/mainfr.uni Klein, Organic Chemistry, 3e CO7T1002478 Give an IUPAC name for the following compound: cycloheptene cyclohexene dy cyclopropene cyclobutene cyclopentene * C trans-3-Methyl-2-pentene C6H gen.wileyplus.com/edugen/student/mainfr.uni JS Klein, Organic Chemistry, 3e CO7T1007433 Which of the following structures could be considered a 4-methyl-1-pentene? LUS Klein, Organic Chemistry, 3e ECES CO7T1002771 Which of the following structures could be considered a 3-heptene? study LUS Klein, Organic Chemistry, 3e RCES COZT10Q2850 Give an IUPAC name for the following compound: (E)-4-hexene (Z)-3-heptene (E)-2-heptene (Z)-4-heptene...
1) Draw structures for compounds named below. A) (2)-1-bromo-2-chloro-1-heptene B) 4-chloro-4-fluoro-2-octyne 2) Give IUPAC name for the following structure. 3) For each reaction below, indicate which starting material is the Nucleophile and which is the Electrophile. Show arrows to demonstrate how the transformation occurs. →^_^tts a Porto ~ onde gi 4) Draw a mechanism for the conversion of the shown starting material to the corresponding product. 5) In the transformation below, a starting material is treated with HCl to form...
lculate the degrees of unsaturation in the following compounds. a. C12H16N302Br b. C8H10C14 c. C9H20N4 d. C15H18 4. Draw structures for the following hydrocarbons. a. 3,5-diethyl-4-isopropyl-2,6-octadiene b. 4,5-dimethyl-1,4,7-decatriene c. 1-chloro-3-bromo-3-heptene d. 2-methyl-1,3-cyclopentadiene e. 4-isopropylcyclohexene
Name or draw the following
Prepare the following using reagents or conditions
necessary.
Name: CHM 2210 Exam 1 Fall 2019 1. Name or draw the following (3 pts each, 18 pts) a. Trans-1,3-Difluorocyclopentane b. (Z)-5-Ethyl-4-isopropyl-1,5-heptadiene c. (3,5E,7Z)-5,7-Diethyl-4-methyl-3,5,7-decatriene that - - hexene d. propyl 2- Bromo-4 propyl t-hexene 3.5-octadiene E e. $23-chloro-6-methyl-3.5-octadiene Me e 3-Ethyl-2-methyl-4-nitro-l-nonene ON nitro ОН Br Br - он All/Br Markou КОН - H₂O H3Rou 2sche + ALI ОН ОН ВСоон BH3 THE ноо оң Arcool-1
JI) Name the compounds or draw the structures from their names. (2 pts) 1,2-chovo mul COOH a) NO2 b) CI c) 4-phenyl-2-pentanol; •DH d) 1-bromo-2-chloro-4-ethylbenzene; 2. Arrange the compounds in each set in order of decreasing reactivity (fastest to slowest) toward EAS. Explain. (2 pts) 0-C-CH3 -C-0-CH3 a) (A) (B) (C) CH2CH3 -NH2 ( C1) do nosotros (B) b) (A) 3. Account for the observation that trifluoromethyl groups is meta directing, as shown in the following example. (1 pt) CF3...
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