Homework Answers
1)Tert butoxide anion abstract the acidic proton and attacks the carbonyl carbon pushing electron pair to oxygen. Then, due to presence of Beta carbonyl (ester) electron pair is pushed towards the ester converting it to the expected product.
2) In the cyclohexane system, base abstract the proton at the junction converting th enolate form. Then, hydride shift takes place in presence of base to form allyl alcohol.Finally, base abstract the proton and dehydration takes place to form the product
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write complete reaction mechanism for the following and explain
steps please
CO E cal to go...
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)
please show all steps 3. For the reaction shown below, only product A was obtained, whereas...
please show all steps
3. For the reaction shown below, only product A was obtained, whereas compound B was not formed. Write the reaction mechanism for the formation of product A and compare its mechanism to the mechanism for the formation of compound B. What conclusion can you draw from your comparison of the mechanisms that would explain why only A and not B is formed? Ph CO E Eto, Ph7 Ph L CO,E! CO,Et 1) NaOET, ETOH 2) HCI...
please help. thanks Q4. Please write the detailed mechanism for the following reaction. Please draw ALL...
please help. thanks
Q4. Please write the detailed mechanism for the following reaction. Please draw ALL CURVY ARROWS charges and electrons. Explain using mechanism which will be major product A or B. (9 pts) Hount . Et and X
3) Write a complete Sn1 mechanism for the following reaction Also, 4) Write a complete Sn2...
3) Write a complete Sn1 mechanism for the following
reaction
Also,
4) Write a complete Sn2 mechanism for the following.
Please show transition state and list a good solvent as well.
Thank you!
3. Write a complete Sn1 mechanism for the following reaction. Вт + CH3OH CH₃CH2 CH3 4. Write a complete SN2 mechanism for the following. Show the transition state as well. Also list a good solvent. OTS + NaCN H3C 3. Write a complete sul mechanism for the...
Give the product for the reaction below and write a complete mechanism: all steps separately. Be...
Give the product for the reaction below and write a complete mechanism: all steps separately. Be sure to show the movement of electron pairs with correct arrows. THE
Please write the steps involved in the proposed reaction mechanism of Haber process?
Please write the steps involved in the proposed reaction mechanism of Haber process?
10. What is the product of the following Diels-Alder reaction? Show the complete arrow pushing mechanism...
10. What is the product of the following Diels-Alder reaction? Show the complete arrow pushing mechanism that accounts for the product. co Et heat CO,Et
I need the mechanism please. IV. Provide a complete stepwise mechanism for the following reaction sequence,...
I need the mechanism please.
IV. Provide a complete stepwise mechanism for the following reaction sequence, including initiation and termination steps for any radical reactions (i.e. write a continuous reaction mechanism with the product of step 1 being used in step 2.... Draw the product of each step in the indicated boxes. 1) Br2, hv 2) KO Bu/BuOH 3) HBr, ROOR Br step 1 product step 2 product
Write the steps in the mechanism and predict the product for the following reaction:
Write the steps in the mechanism and predict the product for the following reaction:
Determine if the reaction is SN1, SN2, E1 or E2. Write the complete mechanism and answer...
Determine if the reaction is SN1, SN2, E1 or E2. Write
the complete mechanism and answer any questions
*Please don't leave any steps out*
но oplommor + NH3- a. Is the most stable alkene formed? Explain b. Is Zaitsev's rule followed? c. If the concentration of substrate is increased will the rate increase, decrease or remain the same? Explain
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)
please show all steps
3. For the reaction shown below, only product A was obtained, whereas compound B was not formed. Write the reaction mechanism for the formation of product A and compare its mechanism to the mechanism for the formation of compound B. What conclusion can you draw from your comparison of the mechanisms that would explain why only A and not B is formed? Ph CO E Eto, Ph7 Ph L CO,E! CO,Et 1) NaOET, ETOH 2) HCI...
please help. thanks
Q4. Please write the detailed mechanism for the following reaction. Please draw ALL CURVY ARROWS charges and electrons. Explain using mechanism which will be major product A or B. (9 pts) Hount . Et and X
3) Write a complete Sn1 mechanism for the following
reaction
Also,
4) Write a complete Sn2 mechanism for the following.
Please show transition state and list a good solvent as well.
Thank you!
3. Write a complete Sn1 mechanism for the following reaction. Вт + CH3OH CH₃CH2 CH3 4. Write a complete SN2 mechanism for the following. Show the transition state as well. Also list a good solvent. OTS + NaCN H3C 3. Write a complete sul mechanism for the...
Give the product for the reaction below and write a complete mechanism: all steps separately. Be sure to show the movement of electron pairs with correct arrows. THE
10. What is the product of the following Diels-Alder reaction? Show the complete arrow pushing mechanism that accounts for the product. co Et heat CO,Et
I need the mechanism please.
IV. Provide a complete stepwise mechanism for the following reaction sequence, including initiation and termination steps for any radical reactions (i.e. write a continuous reaction mechanism with the product of step 1 being used in step 2.... Draw the product of each step in the indicated boxes. 1) Br2, hv 2) KO Bu/BuOH 3) HBr, ROOR Br step 1 product step 2 product
Determine if the reaction is SN1, SN2, E1 or E2. Write
the complete mechanism and answer any questions
*Please don't leave any steps out*
но oplommor + NH3- a. Is the most stable alkene formed? Explain b. Is Zaitsev's rule followed? c. If the concentration of substrate is increased will the rate increase, decrease or remain the same? Explain
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