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.
Homework Answers
Add Answer to:
Treating 2-methyl-1-butene with methanol in the presence of sulfuric acid gives 2-methoxy-2-methylbutane
CH3 CH3 CH3CH2C=CH2 + CH2OH 12304, CH3CH,Ć-OCHz CH3 Treating 2-methyl-1-butene with methanol in the presence of...
CH3 CH3 CH3CH2C=CH2 + CH2OH 12304, CH3CH,Ć-OCHz CH3 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. Arrow-pushing Instructions no XT CH3. HO CH₂ H-ö-CH3
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...
Draw the products of the following reactions, indicating both regiochemistry and stereochemistry when appropriate. draw the...
Draw the products of the following reactions, indicating both
regiochemistry and stereochemistry when appropriate.
draw the organic product(s) expected when this compound
undergoes the Simmons-Smith reaction.
Draw the product of the reaction below.
Reaction of 3-methyl-1-butene with
CH3OH 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.
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
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...
When 2-methyl-3-hexene is treated with Cl2 in methanol, three products are formed (neglecting stereoisomers).
When 2-methyl-3-hexene is treated with Cl2 in methanol, three products are formed (neglecting stereoisomers). Draw curved arrows to show the movement of electrons in this step of the reaction mechanism.
OH ArSO3H + H2O Dihydropyran is synthesized by treating tetrahydrofurfuryl alcohol with an arenesulfonic acid, ArSO...
OH ArSO3H + H2O Dihydropyran is synthesized by treating tetrahydrofurfuryl alcohol with an arenesulfonic acid, ArSO H. Draw curved arrows to show the movement of electrons in this step of the reaction mechanism. Arrow-pushing Instructions Quotes com " --Qat no-X O= O= 0 o= . = O -I
Use curved arrows to propose mechanisms for the following reaction (a)Propene with HCl (b)tert-butylbromide with methanol(c)3-methyl-2-pentene...
Use curved arrows to propose mechanisms for the following reaction (a)Propene with HCl (b)tert-butylbromide with methanol(c)3-methyl-2-pentene with chlorine (d)3-methyl-1-butene with sulphiric acid(e)Propyne with excess HBr (f)2-Pentyne with water in the presence of a mineral acid.
4-hydroxypentanal reacts with one equivalent of methanol to form a cyclic acetal. Draw curved arrows to...
4-hydroxypentanal reacts with one equivalent of methanol to form a cyclic acetal. Draw curved arrows to show the movement of electrons in this step of the reaction mechanism.
1) Give the product for the reaction of 1-butene with methanol in the presence of acid....
1)
Give the product for the reaction of 1-butene with methanol in
the presence of acid. The mechanism is the same as the mechanism
for the addition of water to alkenes.
2-ethoxybutane
1-butanol
2-methoxybutane
1-ethoxybutane
1-methoxybutane
2)
3)
Identify the best nucleophile in an SN2 reaction.
tert-butoxide ion
tert-pentoxide ion
isopropoxide ion
ethoxide ion
4)
Identify the alkyl halide that reacts the fastest in an
SN1 reaction.
2-bromopropane
2-chloropropane
2-iodopropane
2-fluoropropane
What is the major product of the following reaction?...
CH3 CH3 CH3CH2C=CH2 + CH2OH 12304, CH3CH,Ć-OCHz CH3 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. Arrow-pushing Instructions no XT CH3. HO CH₂ H-ö-CH3
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...
Draw the products of the following reactions, indicating both
regiochemistry and stereochemistry when appropriate.
draw the organic product(s) expected when this compound
undergoes the Simmons-Smith reaction.
Draw the product of the reaction below.
Reaction of 3-methyl-1-butene with
CH3OH 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.
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
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...
When 2-methyl-3-hexene is treated with Cl2 in methanol, three products are formed (neglecting stereoisomers). Draw curved arrows to show the movement of electrons in this step of the reaction mechanism.
OH ArSO3H + H2O Dihydropyran is synthesized by treating tetrahydrofurfuryl alcohol with an arenesulfonic acid, ArSO H. Draw curved arrows to show the movement of electrons in this step of the reaction mechanism. Arrow-pushing Instructions Quotes com " --Qat no-X O= O= 0 o= . = O -I
4-hydroxypentanal reacts with one equivalent of methanol to form a cyclic acetal. Draw curved arrows to show the movement of electrons in this step of the reaction mechanism.
1)
Give the product for the reaction of 1-butene with methanol in
the presence of acid. The mechanism is the same as the mechanism
for the addition of water to alkenes.
2-ethoxybutane
1-butanol
2-methoxybutane
1-ethoxybutane
1-methoxybutane
2)
3)
Identify the best nucleophile in an SN2 reaction.
tert-butoxide ion
tert-pentoxide ion
isopropoxide ion
ethoxide ion
4)
Identify the alkyl halide that reacts the fastest in an
SN1 reaction.
2-bromopropane
2-chloropropane
2-iodopropane
2-fluoropropane
What is the major product of the following reaction?...
Most questions answered within 3 hours.
-
When a firm is in an increasing-cost industry, a decrease in
demand will result in economic (Click...
asked 7 minutes ago -
1. Explain what the advantages are of having a System on a Chip
rather than separate...
asked 6 minutes ago -
A turbine is spinning freely at 3750 rpm. It takes 10 min to
coast to a...
asked 10 minutes ago -
home / study / business / operations management / operations
management questions and answers / eastman...
asked 12 minutes ago -
Q1. In a DC machine, if the field winding is replaced by
permanent magnets, can the...
asked 13 minutes ago -
a.) How is a monopolistic firm different from a perfectly
competitive firm? Which firm will have...
asked 32 minutes ago -
The following reagents are available:
Reagent 1: pKa = 5
Reagent 2: pKa = 6.75
Reagent...
asked 32 minutes ago -
A company has entered into a business agreement with a business
partner for managed human resources...
asked 51 minutes ago -
You have been asked to develop a new line of organic skincare
products. Spend time with...
asked 1 hour ago -
Summerdahl Resort's common stock is currently trading at $37 a
share. The stock is expected to...
asked 1 hour ago -
To an economist, the field of industrial organization answers
which of the following questions?
asked 2 hours ago -
How could meeting industry expectations, propel managers into
challenging and possible conflict of interest situations? How...
asked 2 hours ago