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1. Which alkene is the least stable? A 2,4-dimethylpent-2-ene B 2,4-dimethylrent-1-ene C 2.3 dimethylent-2-ene D. 3,4-dimethylpent-2-ene...
1. Which alkene is the least stable? A 2,4-dimethylpent-2-ene B 2,4-dimethylrent-1-ene C 2.3 dimethylent-2-ene D. 3,4-dimethylpent-2-ene E. 3,4-dimethylpent-1-ene A. Solventio B. Hydrogen C. Heat Cap D. Both A a E Both Ba 8. Why is 2. Which is the major product from reaction of sodium iodine with (R)-2-bromo-3-methylbutane in dicholormethane (methylene chloride? A. 2-iodo-2-methylbutane B. 2-methylbut-2-ene C. (S)-2-iodo-3-methyl butante D. 2-methylbut-l-ene E. No Reaction A Atom B. Reso C. Hyb D. Pols E. Indi 3. Which is the major product...
2 Which is the major prodect from reaction of sodiam iodine with (R)-2-bromo-3-methy butane in dicholormethane (met...
2 Which is the major prodect from reaction of sodiam iodine with (R)-2-bromo-3-methy butane in dicholormethane (methylene chioridey A 24odo-2-methy ibutane B. 2-methylbut-2-ene C (S)2-iodo-3-methyl butante D. 2-methylbut-1-ene E No Reaction 3. Which is the major product from reaction of sodium hydroxide with (S)-2-iodo-3,3-dimethylbutane in water? A. 3,3-dimethylbut-1-ene B. 2,4-dimethylbut-2-ene C. 2,4-diemthylbut-1-ene D. 2-methylbut-2-ene E. 2-methylbut-1-ene trl d bste 4. How many potential products from halogenation of 2-phenylbut-2-ene? A. I В. 2 С.3 D. 4 E. 5 2 SN N...
LILULILULU U ULUULLOI CILI I ULIOL PUUDIO 3. (10 points)Show how you would accomplish the following...
LILULILULU U ULUULLOI CILI I ULIOL PUUDIO 3. (10 points)Show how you would accomplish the following synthetic conversions. (a). but-1-ene 1-bromobutane (b). but-1-ene 2-bromobutane ©. 2-methylbutan-2-ol2-bromo-3-methylbutane 4 (10 noints Predict the maior products of the following reactions.
Covert ethylene to acetic acid? 17. Show how you synthesize 4-methyl-hex-2-yne? 18. Convert 2,2-dichloropentane to pent-2-yne?
Covert ethylene to acetic acid? 17. Show how you synthesize 4-methyl-hex-2-yne? 18. Convert 2,2-dichloropentane to pent-2-yne?
1. Show the conditions for and products of an El and E2 reaction with a. cis...
1. Show the conditions for and products of an El and E2 reaction with a. cis and trans iso ne. mers of 1-chloro-2-ethylcyclohexa b. (3R,4R)-4-bromo-3-methylpent-1-ene and it's diastereomer. 2. Which stereoisomer reacts more quickly in E2 reaction - 1R,3R-1-bromo-3- methylcyclohexane, 1S,3S-1-bromo-3-methylcyclohexane, 1R,2S-1-bromo-3- romo-5-methylcyclonexane, methylcyclhexane, 1S,2R-1-bromo-3-methylchyclohexane?
Give the Line Drawing for the followingg (g) 1-chloro-3-methylbutane (h) pentane (1) 2,3-dichloro-2-methylpentane ) 2-chloro-2,4,4-trimethylpentane(k) trichloromethane...
Give the Line Drawing for the followingg (g) 1-chloro-3-methylbutane (h) pentane (1) 2,3-dichloro-2-methylpentane ) 2-chloro-2,4,4-trimethylpentane(k) trichloromethane ()2-butanol (m) 3-methylpentane (n) 3-bromo-2-methylpentane (o) 3-ethylhexane (p) 5-isopropyl-3-methyloctane (q)3,3-dibromo-1,1,1-trichlorobutane (r) cis-1-bromo-2-pentene (s) 2,5-dimethyl-1-hexene (t) 2,5,5-trimethyl-3-heptyne (u) trans-1,2-dibromo-1-butene (v) 2-ethyl-1-butene (w) 5-bromohept-6-en-3-ol (x) 5-methyl-4-hexen-1-yne (v) 3,3-dimethyl-1-butanol (z) butane
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
Show how you would accomplish the following conversions a) trans-hex-3-ene to meso-hexane-3-4-diol. Please explain when to...
Show how you would accomplish the following conversions a)
trans-hex-3-ene to meso-hexane-3-4-diol. Please explain when to
rotate. Thank you !
Show how you would accomplish the following conversions. trans-hex-3-ene to meso-hexane-3,4-diol . ~ CH,C01H HO Chocolate HO rotate CH,CO,H HO HO HO OH Submit Request Answer Part D trans-hex-3-ene to (0,2)-hexane-3,4-diol ~ Ho t do anemie van OSO. rotate racemic (d.1) HO Но он ~ rotate CH CO, HO CHCOM enten met racemic (d.1) HOOH CHICOH HO racemic (d.1) Но...
please help me with questions from 3-10! and the bonus. thank you so much Directions: Place...
please help me with questions from 3-10! and the bonus.
thank you so much
Directions: Place your answers to the following questions in the provided spaces. (12 PTS) 1. What is the hybridization of the carbon atoms numbered 1 and 2 respectively in the following structure? -CU CECH A. B sp,sp? sp, sp sp, sp sp', sp sp, sp Ans. 2. What is the IUPAC name for the molecule shown below? os B. C. D. E. (E)-5-methyl-5-hepten-1-yne (2)-5-methyl-5-hepten-1-yne (E)-3-methyl-2-hepten-6-yne (2)-3-methyl-2-hepten-6-yne...
please help me with Organic Chemistry/Alkynes. Thank you! Directions: Place your answers to the following questio...
please help me with Organic Chemistry/Alkynes. Thank you!
Directions: Place your answers to the following questions in the provided spaces. (12 PTS) 1. What is the hybridization of the carbon atoms numbered 1 and 2 respectively in the following structure? -CI CECH A. B sp,sp? sp?sp? sp, sp sp, sp sp, sp E. Ans. - 2. What is the IUPAC name for the molecule shown below? 6b А. B. (E)-5-methyl-5-hepten-1-yne (2)-5-methyl-5-hepten-1-yne (E)-3-methyl-2-hepten-6-yne (2)-3-methyl-2-hepten-6-yne (E)-2-butynyl-2-butene E. Ans. Select the best explanation...
1. Which alkene is the least stable? A 2,4-dimethylpent-2-ene B 2,4-dimethylrent-1-ene C 2.3 dimethylent-2-ene D. 3,4-dimethylpent-2-ene E. 3,4-dimethylpent-1-ene A. Solventio B. Hydrogen C. Heat Cap D. Both A a E Both Ba 8. Why is 2. Which is the major product from reaction of sodium iodine with (R)-2-bromo-3-methylbutane in dicholormethane (methylene chloride? A. 2-iodo-2-methylbutane B. 2-methylbut-2-ene C. (S)-2-iodo-3-methyl butante D. 2-methylbut-l-ene E. No Reaction A Atom B. Reso C. Hyb D. Pols E. Indi 3. Which is the major product...
2 Which is the major prodect from reaction of sodiam iodine with (R)-2-bromo-3-methy butane in dicholormethane (methylene chioridey A 24odo-2-methy ibutane B. 2-methylbut-2-ene C (S)2-iodo-3-methyl butante D. 2-methylbut-1-ene E No Reaction 3. Which is the major product from reaction of sodium hydroxide with (S)-2-iodo-3,3-dimethylbutane in water? A. 3,3-dimethylbut-1-ene B. 2,4-dimethylbut-2-ene C. 2,4-diemthylbut-1-ene D. 2-methylbut-2-ene E. 2-methylbut-1-ene trl d bste 4. How many potential products from halogenation of 2-phenylbut-2-ene? A. I В. 2 С.3 D. 4 E. 5 2 SN N...
LILULILULU U ULUULLOI CILI I ULIOL PUUDIO 3. (10 points)Show how you would accomplish the following synthetic conversions. (a). but-1-ene 1-bromobutane (b). but-1-ene 2-bromobutane ©. 2-methylbutan-2-ol2-bromo-3-methylbutane 4 (10 noints Predict the maior products of the following reactions.
Covert ethylene to acetic acid? 17. Show how you synthesize 4-methyl-hex-2-yne? 18. Convert 2,2-dichloropentane to pent-2-yne?
1. Show the conditions for and products of an El and E2 reaction with a. cis and trans iso ne. mers of 1-chloro-2-ethylcyclohexa b. (3R,4R)-4-bromo-3-methylpent-1-ene and it's diastereomer. 2. Which stereoisomer reacts more quickly in E2 reaction - 1R,3R-1-bromo-3- methylcyclohexane, 1S,3S-1-bromo-3-methylcyclohexane, 1R,2S-1-bromo-3- romo-5-methylcyclonexane, methylcyclhexane, 1S,2R-1-bromo-3-methylchyclohexane?
Give the Line Drawing for the followingg (g) 1-chloro-3-methylbutane (h) pentane (1) 2,3-dichloro-2-methylpentane ) 2-chloro-2,4,4-trimethylpentane(k) trichloromethane ()2-butanol (m) 3-methylpentane (n) 3-bromo-2-methylpentane (o) 3-ethylhexane (p) 5-isopropyl-3-methyloctane (q)3,3-dibromo-1,1,1-trichlorobutane (r) cis-1-bromo-2-pentene (s) 2,5-dimethyl-1-hexene (t) 2,5,5-trimethyl-3-heptyne (u) trans-1,2-dibromo-1-butene (v) 2-ethyl-1-butene (w) 5-bromohept-6-en-3-ol (x) 5-methyl-4-hexen-1-yne (v) 3,3-dimethyl-1-butanol (z) butane
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
Show how you would accomplish the following conversions a)
trans-hex-3-ene to meso-hexane-3-4-diol. Please explain when to
rotate. Thank you !
Show how you would accomplish the following conversions. trans-hex-3-ene to meso-hexane-3,4-diol . ~ CH,C01H HO Chocolate HO rotate CH,CO,H HO HO HO OH Submit Request Answer Part D trans-hex-3-ene to (0,2)-hexane-3,4-diol ~ Ho t do anemie van OSO. rotate racemic (d.1) HO Но он ~ rotate CH CO, HO CHCOM enten met racemic (d.1) HOOH CHICOH HO racemic (d.1) Но...
please help me with questions from 3-10! and the bonus.
thank you so much
Directions: Place your answers to the following questions in the provided spaces. (12 PTS) 1. What is the hybridization of the carbon atoms numbered 1 and 2 respectively in the following structure? -CU CECH A. B sp,sp? sp, sp sp, sp sp', sp sp, sp Ans. 2. What is the IUPAC name for the molecule shown below? os B. C. D. E. (E)-5-methyl-5-hepten-1-yne (2)-5-methyl-5-hepten-1-yne (E)-3-methyl-2-hepten-6-yne (2)-3-methyl-2-hepten-6-yne...
please help me with Organic Chemistry/Alkynes. Thank you!
Directions: Place your answers to the following questions in the provided spaces. (12 PTS) 1. What is the hybridization of the carbon atoms numbered 1 and 2 respectively in the following structure? -CI CECH A. B sp,sp? sp?sp? sp, sp sp, sp sp, sp E. Ans. - 2. What is the IUPAC name for the molecule shown below? 6b А. B. (E)-5-methyl-5-hepten-1-yne (2)-5-methyl-5-hepten-1-yne (E)-3-methyl-2-hepten-6-yne (2)-3-methyl-2-hepten-6-yne (E)-2-butynyl-2-butene E. Ans. Select the best explanation...
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