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CH3 CH3 CH3CH2C=CH2 + CH2OH 12304, CH3CH,Ć-OCHz CH3 Treating 2-methyl-1-butene with methanol in the presence of...
Treating 2-methyl-1-butene with methanol in the presence of sulfuric acid gives 2-methoxy-2-methylbutane
Treating 2-methyl-1-butene with methanol in the presence of sulfuric acid gives 2-methoxy-2-methylbutane. Draw curved arrows to show the movement of electrons in this step of the reaction mechanism.
can you please draw the number or e- (1 or 2) with the arrows instead of...
can you please draw the number or e- (1 or 2) with the arrows
instead of arrows?
Reaction of 3-methyl-1-butene with CH2OH in the presence of H2SO4 catalyst yields 2-methoxy-2-methylbutane by a mechanism analogous to that of acid- catalyzed alkene hydration. Draw curved arrows to show the movement of electrons in this step of the reaction mechanism. Arrow-pushing Instructions носн y CH3OH amen - Submit Answer Try Another Version 2 item attempts remaining CO2CH3 CO2CH3 Hg(OAC)2 AcOHg Draw curved arrows...
1. Give systematic IUPAC names for each of the following: CH3CH2C(CH3)2CH(CH2CH3)CH3 CH3C(CH3)CH2 CH2O CH3CH(NH2)CH3 CH3OCH2CH2CH3 CH(CH3)2COOH...
1. Give systematic IUPAC names for each of the following:
CH3CH2C(CH3)2CH(CH2CH3)CH3
CH3C(CH3)CH2
CH2O
CH3CH(NH2)CH3
CH3OCH2CH2CH3
CH(CH3)2COOH
For the list above I currently put the following as the IUPAC
names. If any are wrong can you please correct them!
Give systematic IUPAC names for each of the following:
CH3CH2C(CH3)2CH(CH2CH3)CH3
IUPAC Name: 3,3,4-trimethylhexane
IUPAC Name:
3-methyl-4-ol-heptane
CH3C(CH3)CH2 IUPAC Name:
2-methylpropene
CH2O IUPAC Name: methanal
CH3CH(NH2)CH3 IUPAC Name:
isopropylamine
CH3OCH2CH2CH3 IUPAC
Name: methoxyethane (ethyl methyl ether)
CH(CH3)2COOH IUPAC Name:
2-methylpropanoic acid
Reaction of 2-methylpropene with CH3OH in the presence of H2SO4 catalyst yields 2-methoxy-2-methylpropane by a mechanism...
Reaction of 2-methylpropene with CH3OH in the presence of H2SO4 catalyst yields 2-methoxy-2-methylpropane by a mechanism analogous to that of acid-catalyzed alkene hydration. Draw curved arrows to show the movement of electrons in this step of the reaction mechanism. Arrow-pushing Instructions nnex CH3OH OCH — CHJØte er
Chapter 6 [References) Question 5 o 1 pt CH3 CH3 OCH CH3 ÇI CH3 CI Cl2...
Chapter 6 [References) Question 5 o 1 pt CH3 CH3 OCH CH3 ÇI CH3 CI Cl2 CH3CHCH=CHCH2CH3 Question 6 1 pt CH3CHCHCHCH2CH3 SHCHICH.CH CH3CHCHCHCH2CH3 4,снено CHCHCH2CH3 CH3OH Question 7 1 pt CI OCH3 CI Question 8 ® 1 pt When 2-methyl-3-hexene is treated with Cl, in methanol, three products are formed (neglecting stereoisomers). Draw curved arrows to show the movement of electrons in this step of the reaction mechanism. Question 9 1 pt Question 10 1 pt Arrow-pushing Instructions Question...
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. 2. JUST DRAW ARROWS... (CH3)2Culi + CH3Cu Ph CI Ph CH3 The ketone intermediate formed...
1.
2.
JUST DRAW ARROWS...
(CH3)2Culi + CH3Cu Ph CI Ph CH3 The ketone intermediate formed in the reaction of an acid chloride with a Grignard reagent cannot be isolated because it reacts too rapidly with the second equivalent of Grignard reagent. To produce a ketone from an acid chloride, one can treat the acid chloride with a lithium dialkylcopper reagent. The reaction occurs by nucleophilic acyl substitution on the acid chloride by the dialkylcopper anion to yield an acyl...
6) Draw the structure of (Z)-1-chloro-2-methyl-2-butene. 7) Draw the curved arrows to show how CH3CH=CHCH2CH3 reacts...
6) Draw the structure of (Z)-1-chloro-2-methyl-2-butene. 7) Draw the curved arrows to show how CH3CH=CHCH2CH3 reacts with HBr to form a carbocation first, and then forms 2-bromopentane. (this is 2 steps) 7) 8) 8) Predict the product(s) of the following reaction based on the curved arrows: Make sure to include + and- charges where appropriate. -C-NH2 CH CHy HO 9) Based on the following reaction coordinate diagram: Which compound, A or C, is formed faster from B? Which is more...
The acetoacetic ester synthesis is a carbonyl alkylation reaction. It is used to prepare methyl ketones...
The acetoacetic ester synthesis is a carbonyl alkylation reaction. It is used to prepare methyl ketones from primary alkyl halides, lengthening the carbon chain by three atoms. Thus, the product can be visualized as being a "substituted acetone." The reaction consists of three steps: generation of the enolate anion followed by S2 reaction with a primary alkyl halide, ester hydrolysis under acid conditions, and decarboxylation. 1. NaOEt 2. H2O* 3. heat Br + - H₃C + CO2 + ETOH Hc...
CH2 1. (CH2CH2hCuli 2. H30* CH3 The coniugate addition of an alkyl group to an ß-unsaturated...
CH2 1. (CH2CH2hCuli 2. H30* CH3 The coniugate addition of an alkyl group to an ß-unsaturated ketone is one of the more useful 1,4 addition reactions, just as direct additiona more useful 1,2-addition reactions. Conjugate addition occurs via the use of a lithium dialkylcopper reagent, also called a Gilman reagent. The addition of the dialky copper anion to the B-carbon to give a copper-containing intermediate. Transfer of an alkyl group to carbon and release completes the reaction. Draw curved arrows...
Treating 2-methyl-1-butene with methanol in the presence of sulfuric acid gives 2-methoxy-2-methylbutane. Draw curved arrows to show the movement of electrons in this step of the reaction mechanism.
can you please draw the number or e- (1 or 2) with the arrows
instead of arrows?
Reaction of 3-methyl-1-butene with CH2OH in the presence of H2SO4 catalyst yields 2-methoxy-2-methylbutane by a mechanism analogous to that of acid- catalyzed alkene hydration. Draw curved arrows to show the movement of electrons in this step of the reaction mechanism. Arrow-pushing Instructions носн y CH3OH amen - Submit Answer Try Another Version 2 item attempts remaining CO2CH3 CO2CH3 Hg(OAC)2 AcOHg Draw curved arrows...
1. Give systematic IUPAC names for each of the following:
CH3CH2C(CH3)2CH(CH2CH3)CH3
CH3C(CH3)CH2
CH2O
CH3CH(NH2)CH3
CH3OCH2CH2CH3
CH(CH3)2COOH
For the list above I currently put the following as the IUPAC
names. If any are wrong can you please correct them!
Give systematic IUPAC names for each of the following:
CH3CH2C(CH3)2CH(CH2CH3)CH3
IUPAC Name: 3,3,4-trimethylhexane
IUPAC Name:
3-methyl-4-ol-heptane
CH3C(CH3)CH2 IUPAC Name:
2-methylpropene
CH2O IUPAC Name: methanal
CH3CH(NH2)CH3 IUPAC Name:
isopropylamine
CH3OCH2CH2CH3 IUPAC
Name: methoxyethane (ethyl methyl ether)
CH(CH3)2COOH IUPAC Name:
2-methylpropanoic acid
Reaction of 2-methylpropene with CH3OH in the presence of H2SO4 catalyst yields 2-methoxy-2-methylpropane by a mechanism analogous to that of acid-catalyzed alkene hydration. Draw curved arrows to show the movement of electrons in this step of the reaction mechanism. Arrow-pushing Instructions nnex CH3OH OCH — CHJØte er
Chapter 6 [References) Question 5 o 1 pt CH3 CH3 OCH CH3 ÇI CH3 CI Cl2 CH3CHCH=CHCH2CH3 Question 6 1 pt CH3CHCHCHCH2CH3 SHCHICH.CH CH3CHCHCHCH2CH3 4,снено CHCHCH2CH3 CH3OH Question 7 1 pt CI OCH3 CI Question 8 ® 1 pt When 2-methyl-3-hexene is treated with Cl, in methanol, three products are formed (neglecting stereoisomers). Draw curved arrows to show the movement of electrons in this step of the reaction mechanism. Question 9 1 pt Question 10 1 pt Arrow-pushing Instructions Question...
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.
2.
JUST DRAW ARROWS...
(CH3)2Culi + CH3Cu Ph CI Ph CH3 The ketone intermediate formed in the reaction of an acid chloride with a Grignard reagent cannot be isolated because it reacts too rapidly with the second equivalent of Grignard reagent. To produce a ketone from an acid chloride, one can treat the acid chloride with a lithium dialkylcopper reagent. The reaction occurs by nucleophilic acyl substitution on the acid chloride by the dialkylcopper anion to yield an acyl...
6) Draw the structure of (Z)-1-chloro-2-methyl-2-butene. 7) Draw the curved arrows to show how CH3CH=CHCH2CH3 reacts with HBr to form a carbocation first, and then forms 2-bromopentane. (this is 2 steps) 7) 8) 8) Predict the product(s) of the following reaction based on the curved arrows: Make sure to include + and- charges where appropriate. -C-NH2 CH CHy HO 9) Based on the following reaction coordinate diagram: Which compound, A or C, is formed faster from B? Which is more...
The acetoacetic ester synthesis is a carbonyl alkylation reaction. It is used to prepare methyl ketones from primary alkyl halides, lengthening the carbon chain by three atoms. Thus, the product can be visualized as being a "substituted acetone." The reaction consists of three steps: generation of the enolate anion followed by S2 reaction with a primary alkyl halide, ester hydrolysis under acid conditions, and decarboxylation. 1. NaOEt 2. H2O* 3. heat Br + - H₃C + CO2 + ETOH Hc...
CH2 1. (CH2CH2hCuli 2. H30* CH3 The coniugate addition of an alkyl group to an ß-unsaturated ketone is one of the more useful 1,4 addition reactions, just as direct additiona more useful 1,2-addition reactions. Conjugate addition occurs via the use of a lithium dialkylcopper reagent, also called a Gilman reagent. The addition of the dialky copper anion to the B-carbon to give a copper-containing intermediate. Transfer of an alkyl group to carbon and release completes the reaction. Draw curved arrows...
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