Please Help! Write the structural chemical equation for 4-nitroaniline with benzoyl chloride, and draw a detailed...
Please Help! Write the structural chemical equation for 4-nitroaniline with benzoyl chloride, and draw a detailed mechanism with electron pushing arrows.
Homework Answers
Overall reaction is an example for Nucleophilic substitution at acyl group.
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Please Help! Write the structural chemical equation for
4-nitroaniline with benzoyl chloride, and draw a detailed...
Please answer the following two questions 1 and 2. Please answer the following questions 1 and...
Please answer the following two questions 1 and 2.
Please answer the following questions 1 and 2 1. Write the structural chemical equation for the reaction of the given acids with thionyl chloride. a.) Cinnamic Acid + thionyl chloride b.) 4-methoxybenzoic acid + thionyl chloride Write the structural chemical equation for the reaction of your acid chloride from question 2 and aniline for the formation of anilide derivative, and draw out the detailed mechanism with electron pushing arrows. 2.
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
Lookup the structure of styrene and benzoyl peroxide. Write a generic reaction mechanism for the reaction...
Lookup the structure of styrene and benzoyl peroxide. Write a generic reaction mechanism for the reaction of benzoyl peroxide and an alkene like ethylene. (please draw reaction with lone pairs and arrows)
Draw the complete electron-pushing mechanism for each of the reactions. Please draw the reactants, intermediates (with...
Draw the complete electron-pushing mechanism for each of the
reactions. Please draw the reactants, intermediates (with formal
charges), products, and electron-pushing arrows.
1. Draw the complete electron-pushing mechanism for each of the reactions. Please draw the reactants, intermediates (with formal charges), products, and electron-pushing arrows. (6 pts) 2 OH H2O HCI
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
provide the major organic products and draw out detailed mechanism with electron pushing arrows. 1. CH...
provide the major organic products and draw out detailed mechanism
with electron pushing arrows.
1. CH CH CH MgBr 2. H,00 NaBHA CH2CH2OH
H3C Нас H3C CO2H Br 1. NaOH, H20 2 HJo Write a detailed mechanism for the...
H3C Нас H3C CO2H Br 1. NaOH, H20 2 HJo Write a detailed mechanism for the Favorski rearrangement (shown above) which proceeds in two steps followed by a proton transfer. Then draw curved arrows that depict electron reorganization for the mechanism step below Arrow-pushing Instructions IIn OOH H3C H3C Br. :O-H
4) Draw a detailed arrow pushing mechanism for the following transformation. You must show arrows for...
4) Draw a detailed arrow pushing mechanism for the following transformation. You must show arrows for every step, writing statements like "proton transfer without showing the arrows for that step is not an acceptable answer NOE, EIH
Draw the major organic product obtained by reaction of benzoyl chloride with dimethylamine, (CH3)2NH. Please show...
Draw the major organic product obtained by reaction of benzoyl chloride with dimethylamine, (CH3)2NH. Please show the smaller molecular weight molecule and the larger molecular weight molecule. Please show both the products. Thanks
Write a detailed mechanism for the reaction above, then draw curved arrows to detect electron reorganization...
Write a detailed mechanism for the reaction above, then draw curved arrows to detect electron reorganization for the step below. To make a bond to a specific carbon of a double bond, use the "hit box" nearest that carbon.
Please answer the following two questions 1 and 2.
Please answer the following questions 1 and 2 1. Write the structural chemical equation for the reaction of the given acids with thionyl chloride. a.) Cinnamic Acid + thionyl chloride b.) 4-methoxybenzoic acid + thionyl chloride Write the structural chemical equation for the reaction of your acid chloride from question 2 and aniline for the formation of anilide derivative, and draw out the detailed mechanism with electron pushing arrows. 2.
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
Draw the complete electron-pushing mechanism for each of the
reactions. Please draw the reactants, intermediates (with formal
charges), products, and electron-pushing arrows.
1. Draw the complete electron-pushing mechanism for each of the reactions. Please draw the reactants, intermediates (with formal charges), products, and electron-pushing arrows. (6 pts) 2 OH H2O HCI
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
provide the major organic products and draw out detailed mechanism
with electron pushing arrows.
1. CH CH CH MgBr 2. H,00 NaBHA CH2CH2OH
H3C Нас H3C CO2H Br 1. NaOH, H20 2 HJo Write a detailed mechanism for the Favorski rearrangement (shown above) which proceeds in two steps followed by a proton transfer. Then draw curved arrows that depict electron reorganization for the mechanism step below Arrow-pushing Instructions IIn OOH H3C H3C Br. :O-H
4) Draw a detailed arrow pushing mechanism for the following transformation. You must show arrows for every step, writing statements like "proton transfer without showing the arrows for that step is not an acceptable answer NOE, EIH
Write a detailed mechanism for the reaction above, then draw curved arrows to detect electron reorganization for the step below. To make a bond to a specific carbon of a double bond, use the "hit box" nearest that carbon.
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