Homework Answers
Mechanism:
First of all the 2-butanone will react with the H+ and gets activated. Then the pyrolidine ring will attack on the carbonyl center of the 2-butanone and then followed by series of reactions it gives hs the enamine.
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Write out all the steps to show the mechanism upon conversion of 2-butanone to its enamine...
4. Write out all the steps to show the mechanism upon conversion of 2-butanone to its...
4. Write out all the steps to show the mechanism upon conversion of 2-butanone to its enamine under the conditions of acid catalysis. wyn Under normal conditions, treatment of a carboxylic acid with thionyl chloride (SOCl2) gives an acid chloride. However, when butanedioic acid (succinic acid) is exposed to these conditions, a different product is obtained with the molecular formula C4H403. Explain. HA . SOCI, soc, , CH,03 so,
2. Draw out both steps of the malic enzyme mechanism for the conversion of malate to...
2. Draw out both steps of the malic enzyme mechanism for the conversion of malate to pyruvate. Include nicotinamide moieties, acid/base catalysis, and electron movement
please show all steps (a) Write the reaction mechanism for the hydrolysis of the amide under...
please show all steps
(a) Write the reaction mechanism for the hydrolysis of the amide under acidic conditions: 2 Et Н,о° heat OH + EtzNH2 Et (b) Write the reaction mechanism for the base catalyzed hydrolysis of the ester Na +n-BuOH OBu NaOH (aq)
write out the mechanism for the imine formation of 2-butanone (methyl ethyl ketone) with methylamine and...
write out the mechanism for the imine formation of 2-butanone (methyl ethyl ketone) with methylamine and a catalytic amount of sulfuric acid
just want to double check my answers Shit Alt 4. (4 pts.) The mechanism for the...
just want to double check my answers
Shit Alt 4. (4 pts.) The mechanism for the formation of an ester is comprised of the following steps. Identify each of the elementary steps and draw curved arrows to show movement of electrons. Be sure to draw in necessary nonbonding electron pairs +HSO, -S0,H OH нс OH н,с :он H Pro Гон H,C-C AU ie pddihon он 5.advs Н,с. "сн, 2cei он он H Н,с -он OH Нс H,C Palon Thek :0-CHs...
Complete the mechanism for the reaction of butanone hydrate to produce butanone under conditinos of NaOH...
Complete the mechanism for the reaction of butanone hydrate to produce butanone under conditinos of NaOH in water. A reversible reaction takes place, but we will just draw the arrows for formation of the carbonyl in this problem. :0: Hö: OH NaOH H2O :0: Step Step H-Ö ÖH OH : HT Two One :0H Draw the arrows for the 3-step mechanism in formation of the hydrate. (This would not build up and be isolated, but show how it would form.)...
1) a) Write the mechanism for the reaction of butanone with 3-bromobenzaldehyde and NaOH (2:1:1 ratio) b) What is the type of mechanism of this reaction? Consider all resonance structures and AlC...
1) a) Write the mechanism for the reaction of butanone with 3-bromobenzaldehyde and NaOH (2:1:1 ratio) b) What is the type of mechanism of this reaction? Consider all resonance structures and AlCI3. reaction with salicylic acid. 2) Write the mechanism for the reaction of o-toluic acid (CeH&O2) with HNOs and H2SO 3) Write the mechanism for the reaction of 3-Chloro-2-methylbutane with o-nitrophenol 4) Write the mechanism for the reaction of m-nitroanline with NaNO,HCl fllowed by 5) Write the mechanism for...
Write out the complete mechanism and draw all steps and arrows. Draw the product. world N...
Write out the complete mechanism and draw all steps and
arrows. Draw the product.
world N MgBr 1) THE 2) acid
Quickly show all steps and answers all parts of the question please thank you 3. In...
Quickly show all steps and
answers all parts of the question please thank you
3. In the deuterium-labeled compound below predict the product(s) of the elimination reaction of the following elimination reaction and tell whether the alkene formed contains deuterium or not. (20 pts) HCCH; OH H2SO4(aq) heat н,с (ii) NaOCH.CH CH,CH,OH heat CH3 (iii) Write a detail mechanism for the formation of the product in question 3(i).
3 Propose a mechanism for the following reaction. Show all steps Show all nonzero formal charges...
3 Propose a mechanism for the following reaction. Show all steps Show all nonzero formal charges Show all important resonance forms of intermediates Use curved arrows to show electron flow н* NH Ph сн,осн, Hо Ph CH,осH, COCHS CHEGCHS CHyait Ph Ph Ph CHZOC WH3 4. Propose a synthesis of 2-butanol (CH;CHOHCH;CH3) starting with ethanol (CH,CH:OH) as your only source of carbons in the product. You may use any other reagents or solvents as long as they do not contribute...
4. Write out all the steps to show the mechanism upon conversion of 2-butanone to its enamine under the conditions of acid catalysis. wyn Under normal conditions, treatment of a carboxylic acid with thionyl chloride (SOCl2) gives an acid chloride. However, when butanedioic acid (succinic acid) is exposed to these conditions, a different product is obtained with the molecular formula C4H403. Explain. HA . SOCI, soc, , CH,03 so,
2. Draw out both steps of the malic enzyme mechanism for the conversion of malate to pyruvate. Include nicotinamide moieties, acid/base catalysis, and electron movement
please show all steps
(a) Write the reaction mechanism for the hydrolysis of the amide under acidic conditions: 2 Et Н,о° heat OH + EtzNH2 Et (b) Write the reaction mechanism for the base catalyzed hydrolysis of the ester Na +n-BuOH OBu NaOH (aq)
just want to double check my answers
Shit Alt 4. (4 pts.) The mechanism for the formation of an ester is comprised of the following steps. Identify each of the elementary steps and draw curved arrows to show movement of electrons. Be sure to draw in necessary nonbonding electron pairs +HSO, -S0,H OH нс OH н,с :он H Pro Гон H,C-C AU ie pddihon он 5.advs Н,с. "сн, 2cei он он H Н,с -он OH Нс H,C Palon Thek :0-CHs...
Complete the mechanism for the reaction of butanone hydrate to produce butanone under conditinos of NaOH in water. A reversible reaction takes place, but we will just draw the arrows for formation of the carbonyl in this problem. :0: Hö: OH NaOH H2O :0: Step Step H-Ö ÖH OH : HT Two One :0H Draw the arrows for the 3-step mechanism in formation of the hydrate. (This would not build up and be isolated, but show how it would form.)...
1) a) Write the mechanism for the reaction of butanone with 3-bromobenzaldehyde and NaOH (2:1:1 ratio) b) What is the type of mechanism of this reaction? Consider all resonance structures and AlCI3. reaction with salicylic acid. 2) Write the mechanism for the reaction of o-toluic acid (CeH&O2) with HNOs and H2SO 3) Write the mechanism for the reaction of 3-Chloro-2-methylbutane with o-nitrophenol 4) Write the mechanism for the reaction of m-nitroanline with NaNO,HCl fllowed by 5) Write the mechanism for...
Write out the complete mechanism and draw all steps and
arrows. Draw the product.
world N MgBr 1) THE 2) acid
Quickly show all steps and
answers all parts of the question please thank you
3. In the deuterium-labeled compound below predict the product(s) of the elimination reaction of the following elimination reaction and tell whether the alkene formed contains deuterium or not. (20 pts) HCCH; OH H2SO4(aq) heat н,с (ii) NaOCH.CH CH,CH,OH heat CH3 (iii) Write a detail mechanism for the formation of the product in question 3(i).
3 Propose a mechanism for the following reaction. Show all steps Show all nonzero formal charges Show all important resonance forms of intermediates Use curved arrows to show electron flow н* NH Ph сн,осн, Hо Ph CH,осH, COCHS CHEGCHS CHyait Ph Ph Ph CHZOC WH3 4. Propose a synthesis of 2-butanol (CH;CHOHCH;CH3) starting with ethanol (CH,CH:OH) as your only source of carbons in the product. You may use any other reagents or solvents as long as they do not contribute...
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