Identify all of the errors in the mechanism below
Homework Answers
Step1 : No errors. But the secondar carbocation rearranges to more stable tertiary carbo cation.
Step2 : Erros are there. Attached the modified mechanism regadring step2.
Step3 : Errors are there. Attached the modified image below.
The complete mechanism assuming the rearragement to get the stable tertiary carbocation is given in the following image.
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Identify all of the errors in the mechanism below
Label ALL o the errors, ТЕРА Arrows...
Identify errors in the mechanism shown and explain briefly what the errors are and how to...
Identify errors in the mechanism shown and explain briefly what
the errors are and how to fix it. Reference labeled steps and
intermediate structures that have errors to make sure your answer
is clear.
Step 1 Arrows A - Arrows B e AICI, CI-AICI, CI-AICI, Structure 1 Struc Structure 3 Structure 4 Structure 5 Structure 5 Step 2 Arrows D Arrows E Arrows C Structure 7 Structure 8 Structure 9 Structure 10 Arrows G Arrows Arrows Arrows J Structure 7...
Review the following mechanism submitted by a student last spring. Identify the errors in the mechanism...
Review the following mechanism submitted by a student last spring. Identify the errors in the mechanism shown and explain briefly in one concise phrase what the error is and how to fix it. Reference the labeled steps and intermediate structures that have errors to make sure your answer is clear. Arrows A Arrows B Arrows C HO H+ cat. Step 1 Step 2 Structure 1 Structure 2 Structure 3 Step 3 Arrows E Arrows D но Step 5 Step 4...
Draw the mechanism for the reaction shown below: o This mechanism requires 6 distinct steps This...
Draw the mechanism for the reaction shown below: o This mechanism requires 6 distinct steps This is an acid-catalyzed reaction, use the H30+ in your mechanism o Be sure to include all curved arrows to show the movement of electrons Be sure to include all lone pairs and formal charges on atoms, as necessary For each step in your mechanism, label it based on the type of mechanism step it is H H :N-H
Draw the arrows for the 7-step mechanism in formation of the mixed acetal shown. Map CH,OH...
Draw the arrows for the 7-step mechanism in formation of the mixed acetal shown. Map CH,OH OH mi # + HO ht Mixed ACETAL HEMIACETAL click to edit H. 0 Step он H Step w HỘ One H Two HⓇ H H 16 Step 3. Step HÖCH3 Step + H H Five Four Step 6 Draw the arrows for the 7-step mechanism for hydrolysis of an acetal to a carbonyl. Map . H2O Hö: H,O L; E i + CH,CH,OH...
Provide the electron-pushing arrows to complete the mechanism below. Identify the arrow-pushing pattern(s) used in each...
Provide the electron-pushing arrows to complete the mechanism
below. Identify the arrow-pushing pattern(s) used in each step.
(1) Provide electron-pushing arrows to complete the mechanism shown below. Identify the arrow.pushing pattern(s) used at each step. :NH3 H H-NH2 -NH2 NO RO: R R 0 I- -H20 NH2 .NH HN R
Draw the arrows for the 7-step mechanism for hydrolysis of an acetal to a carbonyl. Мар...
Draw the arrows for the 7-step mechanism for hydrolysis of an acetal to a carbonyl. Мар - + CH,CH,OH ACETAL HEMIACETAL 3 Ere X Step Step :0 OH2 H One Two H H H 16 Step 3. Step Step H H H -H Five :0: H Four H H1 Hi H → Step 6 ht H o: Step Draw the arrows for the 7-step mechanism in formation of the mixed acetal shown. Map from СН,ОН OH ܠܢ + HO H...
help with 10 please 10. Consider the three reactions shown below. For each reaction t o...
help with 10 please
10. Consider the three reactions shown below. For each reaction t o 1. Determine whether each of the reactions proceeds via a concerted or a step-wise mechanism. 2. For each concerted reaction, draw the structure of the transition state and label it as transition state (TS). 3. For each step-wise reaction, draw the structure of the most stable intermediate and label it as intermediate. Hint: On the exam, you will need to be able to draw...
Enter the numbers for the mechanism arrows for the SN2 reaction. 8 12 9 H O...
Enter the numbers for the mechanism arrows for the SN2 reaction. 8 12 9 H O 4 5 6 + H3CH2CH2CH2C- 7 Br H3CH2CH2CH2C- OH +
Please draw curved arrows for all 4 steps of the mechanism. Integrated Problem 10.51 The alkyl...
Please draw curved arrows for all 4 steps of the mechanism.
Integrated Problem 10.51 The alkyl hallde 1-bromopropane is one of a number of compounds belng considered as a replacement for chlorofluorocarbons as an Industrial cleaning solvent. In a computational study of its atmospheric oxidatdion products, bromoacetone (structure below) was determined to be the mafor product (J. Phys. Chem. A 2008, 112, 7930 7930). ▼ Step 2 Draw the curved arrows and product for the next step of the mechanism....
identify all reaction mechanism components and provide a forward synethesis and retrosynethesis for the product created....
identify all reaction mechanism components and provide a
forward synethesis and retrosynethesis for the product created.
label all nucleophiles and electrophiles. show and explain how the
product becomes stabilized.
7. Please provide a reasonable mechanism for the transformation below. Be sure to include all intermediates, formal charges, and arrows depicting electron flow. Then, explain the source of stability for the nucleophile in the reaction. (8 points) Org. Lett. 2000 2, 2717. Me. Me. Me Me Me Me Me
Identify errors in the mechanism shown and explain briefly what
the errors are and how to fix it. Reference labeled steps and
intermediate structures that have errors to make sure your answer
is clear.
Step 1 Arrows A - Arrows B e AICI, CI-AICI, CI-AICI, Structure 1 Struc Structure 3 Structure 4 Structure 5 Structure 5 Step 2 Arrows D Arrows E Arrows C Structure 7 Structure 8 Structure 9 Structure 10 Arrows G Arrows Arrows Arrows J Structure 7...
Review the following mechanism submitted by a student last spring. Identify the errors in the mechanism shown and explain briefly in one concise phrase what the error is and how to fix it. Reference the labeled steps and intermediate structures that have errors to make sure your answer is clear. Arrows A Arrows B Arrows C HO H+ cat. Step 1 Step 2 Structure 1 Structure 2 Structure 3 Step 3 Arrows E Arrows D но Step 5 Step 4...
Draw the mechanism for the reaction shown below: o This mechanism requires 6 distinct steps This is an acid-catalyzed reaction, use the H30+ in your mechanism o Be sure to include all curved arrows to show the movement of electrons Be sure to include all lone pairs and formal charges on atoms, as necessary For each step in your mechanism, label it based on the type of mechanism step it is H H :N-H
Draw the arrows for the 7-step mechanism in formation of the mixed acetal shown. Map CH,OH OH mi # + HO ht Mixed ACETAL HEMIACETAL click to edit H. 0 Step он H Step w HỘ One H Two HⓇ H H 16 Step 3. Step HÖCH3 Step + H H Five Four Step 6 Draw the arrows for the 7-step mechanism for hydrolysis of an acetal to a carbonyl. Map . H2O Hö: H,O L; E i + CH,CH,OH...
Provide the electron-pushing arrows to complete the mechanism
below. Identify the arrow-pushing pattern(s) used in each step.
(1) Provide electron-pushing arrows to complete the mechanism shown below. Identify the arrow.pushing pattern(s) used at each step. :NH3 H H-NH2 -NH2 NO RO: R R 0 I- -H20 NH2 .NH HN R
Draw the arrows for the 7-step mechanism for hydrolysis of an acetal to a carbonyl. Мар - + CH,CH,OH ACETAL HEMIACETAL 3 Ere X Step Step :0 OH2 H One Two H H H 16 Step 3. Step Step H H H -H Five :0: H Four H H1 Hi H → Step 6 ht H o: Step Draw the arrows for the 7-step mechanism in formation of the mixed acetal shown. Map from СН,ОН OH ܠܢ + HO H...
help with 10 please
10. Consider the three reactions shown below. For each reaction t o 1. Determine whether each of the reactions proceeds via a concerted or a step-wise mechanism. 2. For each concerted reaction, draw the structure of the transition state and label it as transition state (TS). 3. For each step-wise reaction, draw the structure of the most stable intermediate and label it as intermediate. Hint: On the exam, you will need to be able to draw...
Enter the numbers for the mechanism arrows for the SN2 reaction. 8 12 9 H O 4 5 6 + H3CH2CH2CH2C- 7 Br H3CH2CH2CH2C- OH +
Please draw curved arrows for all 4 steps of the mechanism.
Integrated Problem 10.51 The alkyl hallde 1-bromopropane is one of a number of compounds belng considered as a replacement for chlorofluorocarbons as an Industrial cleaning solvent. In a computational study of its atmospheric oxidatdion products, bromoacetone (structure below) was determined to be the mafor product (J. Phys. Chem. A 2008, 112, 7930 7930). ▼ Step 2 Draw the curved arrows and product for the next step of the mechanism....
identify all reaction mechanism components and provide a
forward synethesis and retrosynethesis for the product created.
label all nucleophiles and electrophiles. show and explain how the
product becomes stabilized.
7. Please provide a reasonable mechanism for the transformation below. Be sure to include all intermediates, formal charges, and arrows depicting electron flow. Then, explain the source of stability for the nucleophile in the reaction. (8 points) Org. Lett. 2000 2, 2717. Me. Me. Me Me Me Me Me
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