Homework Answers
based on the reactant to the product conversion the
possible mechanisms and the steps are as follows
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please show all steps
(a) Write the reaction mechanism for the hydrolysis of the amide under...
Q2. Complete the following base hydrolysis reaction of ester. (1) NaOH (2) (H2O) Q3. Write down...
Q2. Complete the following base hydrolysis reaction of ester. (1) NaOH (2) (H2O) Q3. Write down the base (KOH) catalyzed ester hydrolysis mechanism of the following reaction. OH ol 우
Draw the mechanism for both reactions. The top reaction is Base Catalyzed Ester Hydrolysis and the...
Draw the mechanism for both reactions. The top reaction is Base
Catalyzed Ester Hydrolysis and the bottom is Addition/Elimination
Ester and Amide Mechanisms.
H2O HOR HO 0 H,09
Draw the complete arrow-pushing mechanism. a. Other disaccharides can also be hydrolyzed under acidic conditions. Draw...
Draw the complete arrow-pushing mechanism.
a. Other disaccharides can also be hydrolyzed under acidic conditions. Draw the complete arrow-pushing mechanism (including curved arrows, formal charges, and important resonance contributors) for the acid-catalyzed hydrolysis of the disaccharide shown below to give the products shown (note the coefficient!). СН,ОН — о СН,ОН о н н н н КВН н 8н н . нсі (ад.), Н,0 80 °C , СН,ОН но, н , Bн н . Он и он н Он н ....
4. Conversion of B into C involves hydrolysis of the ester followed by decarboxylation. On the...
4. Conversion of B into C involves hydrolysis of the ester followed by decarboxylation. On the structures provided below, show the electron flow for the decarboxylation step. CH2Ph 5. The initial product formed on decarboxylation is an enol, which rapidly equilibrates to its keto form under the acidic reaction conditions. Write the complete stepwise mechanism for the acid-catalyzed conversion of the enol into its keto form, Compound C. Ph Ph
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).
Please write the mechanism for the acid catalyzed hydrolysis of this compound. Show intermediates, formal charges,...
Please write the mechanism for the acid catalyzed hydrolysis
of this compound. Show intermediates, formal charges, and lone
pairs. Use curvy arrows.
0
Please show the mechanism with acid. 2. Write the complete reaction mechanism for the KCN-catalyzed reaction....
Please show the mechanism with acid.
2. Write the complete reaction mechanism for the KCN-catalyzed reaction. Show all electron flow with arrows and show all intermediate structures он CH-COOH O но CN = C H20* Who. HHCEN NAOH HO cyanolydrin + NaCN + H2O
need help with the mechanism must include all steps and show all curly arrows and workings....
need help with the mechanism must include all steps and show all
curly arrows and workings.
+ Meo, co Me (1) NaOH Naome Ovo (1) HCIO MeOH X CO,Me () heat NB: When writing the mechanism for dimedone formation you need to include all of the following steps (i) the Michael addition, (ii) the Dieckmann condensation, (iii) the hydrolysis of the ester and (iv) the decarboxylation of the B-keto acid
Write out all the steps to show the mechanism upon conversion of 2-butanone to its enamine...
Write out all the steps to show the mechanism upon conversion of 2-butanone to its enamine under the conditions of acid catalysis. 4. .CH нс .CH Н,с"
please show mechanism arrows with steps 4. Determine the product of the following epoxide reaction in...
please show mechanism arrows with steps
4. Determine the product of the following epoxide reaction in acidic conditions: CH3OH H2SO4 (trace)
Q2. Complete the following base hydrolysis reaction of ester. (1) NaOH (2) (H2O) Q3. Write down the base (KOH) catalyzed ester hydrolysis mechanism of the following reaction. OH ol 우
Draw the mechanism for both reactions. The top reaction is Base
Catalyzed Ester Hydrolysis and the bottom is Addition/Elimination
Ester and Amide Mechanisms.
H2O HOR HO 0 H,09
Draw the complete arrow-pushing mechanism.
a. Other disaccharides can also be hydrolyzed under acidic conditions. Draw the complete arrow-pushing mechanism (including curved arrows, formal charges, and important resonance contributors) for the acid-catalyzed hydrolysis of the disaccharide shown below to give the products shown (note the coefficient!). СН,ОН — о СН,ОН о н н н н КВН н 8н н . нсі (ад.), Н,0 80 °C , СН,ОН но, н , Bн н . Он и он н Он н ....
4. Conversion of B into C involves hydrolysis of the ester followed by decarboxylation. On the structures provided below, show the electron flow for the decarboxylation step. CH2Ph 5. The initial product formed on decarboxylation is an enol, which rapidly equilibrates to its keto form under the acidic reaction conditions. Write the complete stepwise mechanism for the acid-catalyzed conversion of the enol into its keto form, Compound C. Ph Ph
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).
Please write the mechanism for the acid catalyzed hydrolysis
of this compound. Show intermediates, formal charges, and lone
pairs. Use curvy arrows.
0
Please show the mechanism with acid.
2. Write the complete reaction mechanism for the KCN-catalyzed reaction. Show all electron flow with arrows and show all intermediate structures он CH-COOH O но CN = C H20* Who. HHCEN NAOH HO cyanolydrin + NaCN + H2O
need help with the mechanism must include all steps and show all
curly arrows and workings.
+ Meo, co Me (1) NaOH Naome Ovo (1) HCIO MeOH X CO,Me () heat NB: When writing the mechanism for dimedone formation you need to include all of the following steps (i) the Michael addition, (ii) the Dieckmann condensation, (iii) the hydrolysis of the ester and (iv) the decarboxylation of the B-keto acid
Write out all the steps to show the mechanism upon conversion of 2-butanone to its enamine under the conditions of acid catalysis. 4. .CH нс .CH Н,с"
please show mechanism arrows with steps
4. Determine the product of the following epoxide reaction in acidic conditions: CH3OH H2SO4 (trace)
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