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The given unknown compound is 2-chloro-2,3-dimethylbutane
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6. An unknown compound with molecular formula CH CI is treated with sodium methoxide to produce 2,3-dimethyl-2-bute...
An unknown compound with molecular formula CHC1 is treated with sodium methoxide to produce 2,3-dimethyl-2-butene as...
An unknown compound with molecular formula CHC1 is treated with sodium methoxide to produce 2,3-dimethyl-2-butene as the major product. Identify the structure of the unknown compound (20pts). 6.
Question 40 Get help answering Molecular Drawing questions. Your answer is partially correct. Try again. Compound...
Question 40 Get help answering Molecular Drawing questions. Your answer is partially correct. Try again. Compound A and compound B are constitutional isomers with molecular formula C4H9Cl. Treatment of compound A with sodium methoxide gives trans-2- butene as the major product, while treatment of compound B with sodium methoxide gives a different disubstituted alkene as the major product. Draw the structure of compound A. CH3 HzĆ CI Propose two structures for compound B. H&C CH2 Edit HC H3
2. (12 pt) Unknown compound has a molecular formula of CH.0. The proton NMR spectra presented...
2. (12 pt) Unknown compound has a molecular formula of CH.0. The proton NMR spectra presented below. Identify substructures (explain why) and draw your final solution in the space provided CH 3,482 H
1) When 3-iodo-3-ethylpentane is treated with sodium methoxide in methanol, the major organic product is an...
1) When 3-iodo-3-ethylpentane is treated with sodium methoxide in methanol, the major organic product is an ___that is generated through an __mechanism. A) ether, Sw1 B) ether, SN2 C) ether, E1 D) alkene, E2 E) alkene, E1 2) Which compound produces only one alkene when treated with sodium methoxide? A) 2-chloro-2-methylpentane B) 3-chloro-3-ethylpentane C) 3-chloro-2-methylpentane D) 2-chloro-4-methylpentane E) 2-chloro-3-ethylpentane 3) What is the difference between Hoffmann and Zaitsev? When is Hoffmann favored?
1) When 3-iodo-3-ethylpentane is treated with sodium methoxide in methanol, the major organic product is an...
1) When 3-iodo-3-ethylpentane is treated with sodium methoxide in methanol, the major organic product is an ___ that is generated through an ____mechanism. A) ether, SN1 B) ether, Sn2 C) ether, E1 D) alkene, E2 E) alkene, E1 2) Which compound produces only one alkene when treated with sodium methoxide? A) 2-chloro-2-methylpentane B) 3-chloro-3-ethylpentane C) 3-chloro-2-methylpentane D) 2-chloro-4-methylpentane E) 2-chloro-3-ethylpentane 3) What is the difference between Hoffmann and Zaitsev? When is Hoffmann favored?
6. Treatment of 1 mole ot dimethyl sulfate with 2 moles of sodium acetylide results in the format...
6. Treatment of 1 mole ot dimethyl sulfate with 2 moles of sodium acetylide results in the formation of two moles of propyne as the major product. Draw a reasonable mechanism accounting for the formation of the byproduct 2-butyne. J. Org. Chem. 1959, 24, 840-842. (12 points) major product (2 moles) byproduct (1 equiv) (2 equiv) 7. At high temperatures, alkanes can undergo dehydrogentation to produce alkenes. This reaction is used industrially to prep Explain why dehydrogenation only works at...
1) An unknown organic compound has the molecular formula C4H10O. It resists oxidation and it can...
1) An unknown organic compound has the molecular formula C4H10O. It resists oxidation and it can undergo dehydration to form an alkene.Draw the structure for the compound and write equations for the reactions described. Name the reactant and product. 2) An unknown organic compound has the molecular formula C4H8O. It resists oxidation and it can be reduced with H2 to form an alcohol. Draw the structure for the compound and write equations for the reactions described. Name the reactant and...
1. What is the IUPAC name for the following compound? CH3 CI CH3-CH-C- CH-CH CH3 CH3...
1. What is the IUPAC name for the following compound? CH3 CI CH3-CH-C- CH-CH CH3 CH3 A) 4-chloro-4,5-dimethyl-2-hexene B) 3-chloro-1,3,4-trimethyl-1-pentene C) 3-chloro-2,3-dimethyl-4-hexene D) 3-chloro-2,3,5-trimethyl-4-pentene E) 3-chloro-1,3,4,4-tetramethyl-1-butene 2. Name the following compound. CH-CH2 CH,CH CH CCH H-CH A) 2,2-diethylpenatane B) 2,2-diethylpentene C) 4-ethyl-4-methyl-5-hexene D) 3-ethyl-3-methyl-1-hexene E) 4-ethyl-4-methylhexane 3. Name the following compound. CH CH CH, CH,CH CC CH CH2CH CH A) 3-butyl-3-propyl-1-pentyne B) 3-butyl-3-propyl-4-pentyne C) 3-ethyl-3-propyl-1-heptyne D) 5-ethyl-5-propyl-6-heptyne E) 3-ethyl-3-butyl-1-hexyne
Question 58 3 pts **WRITTEN WORK** An unknown compound with a molecular formula CH,O2 produced the...
Question 58 3 pts **WRITTEN WORK** An unknown compound with a molecular formula CH,O2 produced the IR spectrum shown here. Draw a structure that is consistent with the spectrum. 3 FE HTML Editor ill all x XEE
need help on the last hw problems please explain and answer 43. An unknown compound of...
need help on the last hw problems please explain and
answer
43. An unknown compound of formula CeH16 was found to be optically active. On catalytic reduction of the unknown compound over a palladium catalyst, 2 equivalents of hydrogen were absorbed. Ozonolysis of the unknown compound gave two products: one was identified as an optically active dialdehyde of formula CsHaO2; the other compound was identified as acetaldehyde (CH3CHO). The most likely structure of the unknown compound is B. CH.CH-CH-CHECH CH...
An unknown compound with molecular formula CHC1 is treated with sodium methoxide to produce 2,3-dimethyl-2-butene as the major product. Identify the structure of the unknown compound (20pts). 6.
Question 40 Get help answering Molecular Drawing questions. Your answer is partially correct. Try again. Compound A and compound B are constitutional isomers with molecular formula C4H9Cl. Treatment of compound A with sodium methoxide gives trans-2- butene as the major product, while treatment of compound B with sodium methoxide gives a different disubstituted alkene as the major product. Draw the structure of compound A. CH3 HzĆ CI Propose two structures for compound B. H&C CH2 Edit HC H3
2. (12 pt) Unknown compound has a molecular formula of CH.0. The proton NMR spectra presented below. Identify substructures (explain why) and draw your final solution in the space provided CH 3,482 H
1) When 3-iodo-3-ethylpentane is treated with sodium methoxide in methanol, the major organic product is an ___that is generated through an __mechanism. A) ether, Sw1 B) ether, SN2 C) ether, E1 D) alkene, E2 E) alkene, E1 2) Which compound produces only one alkene when treated with sodium methoxide? A) 2-chloro-2-methylpentane B) 3-chloro-3-ethylpentane C) 3-chloro-2-methylpentane D) 2-chloro-4-methylpentane E) 2-chloro-3-ethylpentane 3) What is the difference between Hoffmann and Zaitsev? When is Hoffmann favored?
1) When 3-iodo-3-ethylpentane is treated with sodium methoxide in methanol, the major organic product is an ___ that is generated through an ____mechanism. A) ether, SN1 B) ether, Sn2 C) ether, E1 D) alkene, E2 E) alkene, E1 2) Which compound produces only one alkene when treated with sodium methoxide? A) 2-chloro-2-methylpentane B) 3-chloro-3-ethylpentane C) 3-chloro-2-methylpentane D) 2-chloro-4-methylpentane E) 2-chloro-3-ethylpentane 3) What is the difference between Hoffmann and Zaitsev? When is Hoffmann favored?
6. Treatment of 1 mole ot dimethyl sulfate with 2 moles of sodium acetylide results in the formation of two moles of propyne as the major product. Draw a reasonable mechanism accounting for the formation of the byproduct 2-butyne. J. Org. Chem. 1959, 24, 840-842. (12 points) major product (2 moles) byproduct (1 equiv) (2 equiv) 7. At high temperatures, alkanes can undergo dehydrogentation to produce alkenes. This reaction is used industrially to prep Explain why dehydrogenation only works at...
1. What is the IUPAC name for the following compound? CH3 CI CH3-CH-C- CH-CH CH3 CH3 A) 4-chloro-4,5-dimethyl-2-hexene B) 3-chloro-1,3,4-trimethyl-1-pentene C) 3-chloro-2,3-dimethyl-4-hexene D) 3-chloro-2,3,5-trimethyl-4-pentene E) 3-chloro-1,3,4,4-tetramethyl-1-butene 2. Name the following compound. CH-CH2 CH,CH CH CCH H-CH A) 2,2-diethylpenatane B) 2,2-diethylpentene C) 4-ethyl-4-methyl-5-hexene D) 3-ethyl-3-methyl-1-hexene E) 4-ethyl-4-methylhexane 3. Name the following compound. CH CH CH, CH,CH CC CH CH2CH CH A) 3-butyl-3-propyl-1-pentyne B) 3-butyl-3-propyl-4-pentyne C) 3-ethyl-3-propyl-1-heptyne D) 5-ethyl-5-propyl-6-heptyne E) 3-ethyl-3-butyl-1-hexyne
Question 58 3 pts **WRITTEN WORK** An unknown compound with a molecular formula CH,O2 produced the IR spectrum shown here. Draw a structure that is consistent with the spectrum. 3 FE HTML Editor ill all x XEE
need help on the last hw problems please explain and
answer
43. An unknown compound of formula CeH16 was found to be optically active. On catalytic reduction of the unknown compound over a palladium catalyst, 2 equivalents of hydrogen were absorbed. Ozonolysis of the unknown compound gave two products: one was identified as an optically active dialdehyde of formula CsHaO2; the other compound was identified as acetaldehyde (CH3CHO). The most likely structure of the unknown compound is B. CH.CH-CH-CHECH CH...
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