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Conversion of 3° alcohols into 3° alkyl halides under acidic conditions involves three steps and two...
Please draw the major product for this reaction I drew this and it said it waas...
Please draw the major product for this reaction I drew this and
it said it waas wrong please help, thanks
Conversion of tertiary alcohols to alkenes under acidic conditions involves two cationic intermediates. For the reaction below: OH Hao a Write a mechanism for the step below using curved arrows to show electron reorganization. Arrow-pushing Instructions H Ob Draw the organic product of the mechanism step above Do not include counter-ions, e.g., Na IT, in your answer.
1. NaOEt CO2Et 2. H30+ 3. heat Br. Br CORET + H3C V CO2H H₂C +...
1. NaOEt CO2Et 2. H30+ 3. heat Br. Br CORET + H3C V CO2H H₂C + CO2 + E H3C CO2Et The malonic ester synthesis is a carbonyl alkylation reaction. It is used to prepare carboxylic acids from primary alkyl halides, lengthening the carbon In progress by two atoms. Thus, the product can be visualized as being a "substituted acetic acid." The reaction consists of three steps: generation of the enolate anion followed by SN 2 reaction with a primary...
Please, make the answer clear and reable. BrEtOH a OEt Hace H2C Alkyl halides undergo nucleophilic...
Please, make the answer clear
and reable.
BrEtOH a OEt Hace H2C Alkyl halides undergo nucleophilic substitution and elimination reactions. When the kinetics of the reaction are measured, if the rate of the reaction is found to be dependent only upon the concentration of the alkyl halide the reaction is first order. The substitution reaction is thus termed ction is termed E1. These reactions are unimolecular and occur in two steps. The first step is rate-limiting and involves the loss...
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...
Write a detailed mechanism for the reaction of dimethylamine in water with acetic anhydride to create...
Write a detailed mechanism for the reaction of dimethylamine in water with acetic anhydride to create N,N-dimethylacetamide which proceeds in 3 steps including proton transfer steps. Then draw curved arrows that depict electron reorganization for the mechanism step below. Arrow-pushing Instructions nno XT :0: :0 H CH3 :N-Me 1 нс N-Me Me Me
The electrophilic addition reaction shown below involves a carbocation rearrangement.
The electrophilic addition reaction shown below involves a
carbocation rearrangement. For the mechanism step below, draw
curved arrows to show electron reorganization. use the arrow tool
to specify the origin and the destination of the reorganizing
electrons.Consult the arrow-pushing instructions for the convention on regiospecific electrophilic attack on a double bond
Hydration of alkenes under aqueous acidic conditions. Draw the detailed stepwise mechanism for this reaction. Be...
Hydration of alkenes under aqueous acidic conditions. Draw the detailed stepwise mechanism for this reaction. Be sure to show all steps, intermediates, formal charges, and show the movement of electrons with curved arrows. You do not need to draw transition states. H2SO4 H20 ?? The hydration of alkynes can also occur under aqueous acidic conditions however, instead of forming the alcohol, a ketone is formed. Draw the detailed stepwise mechanism for the conversion of the alkyne to the ketone (one...
13 SN1: Synthesis of tert-Butyl Chloride Alkyl halides can be prepared from their corresponding alcohols via...
13 SN1: Synthesis of tert-Butyl Chloride Alkyl halides can be prepared from their corresponding alcohols via an acid catalyzed substitution reaction. The mechanism of these acid catalyzed substitution reactions are labeled as Syl (substitution, nucleophilic, unimolecular) and S2 (substitution, nucleophilic, bimolecular). Tertiary alcohols follow the Snl route, primary alcohols follow the S2 route, and secondary alcohols can follow either path. Under acidic conditions, the mechanism (Figure 1) of the Sul reaction involves rapid protonation of the alcohol, followed by the...
LILIT OH O Но Ethylene oxide is the starting material for the synthesis of 1,4-dioxane. Write...
LILIT OH O Но Ethylene oxide is the starting material for the synthesis of 1,4-dioxane. Write a detailed mechanism for this synthesis (shown above). Then draw curved arrows that depict electron reorganization for Step 1 of the mechanism shown below. Unless specified otherwise, do not count proton transfers when counting steps. The starting materials of this step are provided. Arrow-pushing Instructions in + XT H₂C- CH₂
13 SN1: Synthesis of tert-Butyl Chloride Alkyl halides can be prepared from their corresponding alcohols via...
13 SN1: Synthesis of tert-Butyl Chloride Alkyl halides can be prepared from their corresponding alcohols via an acid catalyzed substitution reaction. The mechanism of these acid catalyzed substitution reactions are labeled as Syl (substitution, nucleophilic, unimolecular) and S2 (substitution, nucleophilic, bimolecular). Tertiary alcohols follow the Snl route, primary alcohols follow the S2 route, and secondary alcohols can follow either path. Under acidic conditions, the mechanism (Figure 1) of the Sul reaction involves rapid protonation of the alcohol, followed by the...
Please draw the major product for this reaction I drew this and
it said it waas wrong please help, thanks
Conversion of tertiary alcohols to alkenes under acidic conditions involves two cationic intermediates. For the reaction below: OH Hao a Write a mechanism for the step below using curved arrows to show electron reorganization. Arrow-pushing Instructions H Ob Draw the organic product of the mechanism step above Do not include counter-ions, e.g., Na IT, in your answer.
1. NaOEt CO2Et 2. H30+ 3. heat Br. Br CORET + H3C V CO2H H₂C + CO2 + E H3C CO2Et The malonic ester synthesis is a carbonyl alkylation reaction. It is used to prepare carboxylic acids from primary alkyl halides, lengthening the carbon In progress by two atoms. Thus, the product can be visualized as being a "substituted acetic acid." The reaction consists of three steps: generation of the enolate anion followed by SN 2 reaction with a primary...
Please, make the answer clear
and reable.
BrEtOH a OEt Hace H2C Alkyl halides undergo nucleophilic substitution and elimination reactions. When the kinetics of the reaction are measured, if the rate of the reaction is found to be dependent only upon the concentration of the alkyl halide the reaction is first order. The substitution reaction is thus termed ction is termed E1. These reactions are unimolecular and occur in two steps. The first step is rate-limiting and involves the loss...
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...
Write a detailed mechanism for the reaction of dimethylamine in water with acetic anhydride to create N,N-dimethylacetamide which proceeds in 3 steps including proton transfer steps. Then draw curved arrows that depict electron reorganization for the mechanism step below. Arrow-pushing Instructions nno XT :0: :0 H CH3 :N-Me 1 нс N-Me Me Me
Hydration of alkenes under aqueous acidic conditions. Draw the detailed stepwise mechanism for this reaction. Be sure to show all steps, intermediates, formal charges, and show the movement of electrons with curved arrows. You do not need to draw transition states. H2SO4 H20 ?? The hydration of alkynes can also occur under aqueous acidic conditions however, instead of forming the alcohol, a ketone is formed. Draw the detailed stepwise mechanism for the conversion of the alkyne to the ketone (one...
13 SN1: Synthesis of tert-Butyl Chloride Alkyl halides can be prepared from their corresponding alcohols via an acid catalyzed substitution reaction. The mechanism of these acid catalyzed substitution reactions are labeled as Syl (substitution, nucleophilic, unimolecular) and S2 (substitution, nucleophilic, bimolecular). Tertiary alcohols follow the Snl route, primary alcohols follow the S2 route, and secondary alcohols can follow either path. Under acidic conditions, the mechanism (Figure 1) of the Sul reaction involves rapid protonation of the alcohol, followed by the...
LILIT OH O Но Ethylene oxide is the starting material for the synthesis of 1,4-dioxane. Write a detailed mechanism for this synthesis (shown above). Then draw curved arrows that depict electron reorganization for Step 1 of the mechanism shown below. Unless specified otherwise, do not count proton transfers when counting steps. The starting materials of this step are provided. Arrow-pushing Instructions in + XT H₂C- CH₂
13 SN1: Synthesis of tert-Butyl Chloride Alkyl halides can be prepared from their corresponding alcohols via an acid catalyzed substitution reaction. The mechanism of these acid catalyzed substitution reactions are labeled as Syl (substitution, nucleophilic, unimolecular) and S2 (substitution, nucleophilic, bimolecular). Tertiary alcohols follow the Snl route, primary alcohols follow the S2 route, and secondary alcohols can follow either path. Under acidic conditions, the mechanism (Figure 1) of the Sul reaction involves rapid protonation of the alcohol, followed by the...
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