A.) Draw the mechanism of the first part of the reaction to make the isocyanate, making sure you account for all steps in the mechanism.
B.) Draw the mechanism of the second part of the reaction to make the amine, making sure you account for all steps of the mechanism.
Please answer both parts thanks!
Homework Answers
Add Answer to:
A.) Draw the mechanism of the first part of the reaction to make
the isocyanate, making...
(a) Draw the mechanism of the first part of the reaction to make the isocyanate, making...
(a) Draw the mechanism of the first part of the reaction to
make the isocyanate, making sure you account for all steps in the
mechanism.
(b) Draw the mechanism of the second part of the reaction to
make the amine, making sure you account for all steps in the
mechanism.
household bleach in basic solution. In this experiment, you will synthesize 3-nitroaniline via a mild Hofmann rearrangement with bleach. ON NaOCI (5%) NaOH isocyanate intermediate Figure 1. Reaction Scheme. .
NaOCI (5%) N ON NH2 NH2 NaOH isocyanate intermediate Figure 1. Reaction Scheme. 1) Fill in...
NaOCI (5%) N ON NH2 NH2 NaOH isocyanate intermediate Figure 1. Reaction Scheme. 1) Fill in the reaction table below. Make sure you correctly calculate the molar amounts of your reactants. name formula mol.-eg. Mw mmol amount 3-nitrobenzamide 1.0 g 9.0 mL 5.75% Bleach (aq.) 1 M Aqueous NaOH 12 mL product 2) Calculate the Theoretical Yield of your product, i.e. the mass you would expect to recover (assuming 100% conversion to product).
If you could answer 1 and 2 please. Thanks! Introduction One of the best ways to...
If you could answer 1 and 2 please. Thanks!
Introduction One of the best ways to make aromatic amines is to exploit a rearrangement reaction that breaks a C-C bond. To achieve the rearrangement, you need to make an acyl nitrene intermediate (or suitable derivative). There are a variety of these processes: the Curtius and Schmidt rearrangements access the nitrenes from acyl azides, but these can be explosive, so aren't ideal for an undergraduate lab. The other method is to...
(10 points) Draw the correct product for the reaction below. For step 2, draw the reaction...
(10 points) Draw the correct product for the reaction below. For step 2, draw the reaction mechanism. Be sure to include important intermediate compounds, electron flow arrows, and formal charges for full credit. ОН 1. SOCl2, pyridine 2. CH3NH2 (10 points) Fill in the boxes with the missing starting material, intermediate products, reagents, and/or products. Then for each reaction draw the reaction mechanism with Correct electron flow arrows if appropriate or intermediates and correct formal charges. -OH -NH2 NH (10...
Draw the reaction and reaction mechanism for the reaction of both cis and trans stilbene with...
Draw the reaction and reaction mechanism for the reaction of
both
cis
and
trans
stilbene with Br2
as part of your prelab procedure.
Note: I'm not sure what the
mechanisms look like so that's why I'm having trouble with the
products. Please, if you can, draw out the mechanisms for both of
these!! Thanks.
cis-stilbene trans-stilbene
Making sure to show all steps and arrows, draw a plausible mechanism from the transformation shown...
Making sure to show all steps and arrows, draw a plausible
mechanism from the transformation shown below.
1) Making sure to show all steps and arrows, draw a plausible mechanism for the transformation shown below. (10 points) ОН - &- + HBr Br
Draw a plausible mechanism??? help please! 1) Making sure to show all steps and arrows, draw...
Draw a plausible mechanism??? help please!
1) Making sure to show all steps and arrows, draw a plausible mechanism for the transformation show below. (10 points) + HBr
PART III. Mechanism problems 38. Please draw a plausible reaction mechanism of solvolysis reaction by showing...
PART III. Mechanism problems 38. Please draw a plausible reaction mechanism of solvolysis reaction by showing poessbility of reermeer ned ntemesatws with the mao prmist. If there isa possibility of rearrangement, please show it for the major product CH3 39. Propose a detailed, step-by-step mechanism for the reaction pathway shown below. 40. CH,CH,CH,Br+NaCCC 41. Plcase draw a plausible reaction mechanism of the following free radical reaction by showing the initiation step, propagation step, and termination step. Bry
I need to know the mechanism for step 1- it should be detailed showing all curved...
I need to know the mechanism for step 1- it should be
detailed showing all curved arrows and the correct molecular
structures for reactants, intermediates, and products. thank you
for your help!
2. Nitration and the Hofmann Rearrangement Monk, K.A.; Mohan R.S. The Hofmann Rearrangement Using Househo Synthesis of 3-Nitroaniline). Chem. Educ. 1999,76,1717 and McElveen, vardinas, K.; Stamberger, J.A.: Mohan. R.S. The Discovery-Oriented Approach Organic Chemistry 1. Nitration of Unknown Organic Compounds.). Chem. 1999, 76,535-536.) Step 1. Preparation of 3-nitrobenzamide...
Draw the Mechanism for the following reaction. Make sure to have correct stereochemistry and proper structure...
Draw the Mechanism for the following reaction. Make sure to have correct stereochemistry and proper structure in all your structures. You may show just one sterosome throughout your mechanism, but provide all possibilities in your final answer
(a) Draw the mechanism of the first part of the reaction to
make the isocyanate, making sure you account for all steps in the
mechanism.
(b) Draw the mechanism of the second part of the reaction to
make the amine, making sure you account for all steps in the
mechanism.
household bleach in basic solution. In this experiment, you will synthesize 3-nitroaniline via a mild Hofmann rearrangement with bleach. ON NaOCI (5%) NaOH isocyanate intermediate Figure 1. Reaction Scheme. .
NaOCI (5%) N ON NH2 NH2 NaOH isocyanate intermediate Figure 1. Reaction Scheme. 1) Fill in the reaction table below. Make sure you correctly calculate the molar amounts of your reactants. name formula mol.-eg. Mw mmol amount 3-nitrobenzamide 1.0 g 9.0 mL 5.75% Bleach (aq.) 1 M Aqueous NaOH 12 mL product 2) Calculate the Theoretical Yield of your product, i.e. the mass you would expect to recover (assuming 100% conversion to product).
If you could answer 1 and 2 please. Thanks!
Introduction One of the best ways to make aromatic amines is to exploit a rearrangement reaction that breaks a C-C bond. To achieve the rearrangement, you need to make an acyl nitrene intermediate (or suitable derivative). There are a variety of these processes: the Curtius and Schmidt rearrangements access the nitrenes from acyl azides, but these can be explosive, so aren't ideal for an undergraduate lab. The other method is to...
(10 points) Draw the correct product for the reaction below. For step 2, draw the reaction mechanism. Be sure to include important intermediate compounds, electron flow arrows, and formal charges for full credit. ОН 1. SOCl2, pyridine 2. CH3NH2 (10 points) Fill in the boxes with the missing starting material, intermediate products, reagents, and/or products. Then for each reaction draw the reaction mechanism with Correct electron flow arrows if appropriate or intermediates and correct formal charges. -OH -NH2 NH (10...
Draw the reaction and reaction mechanism for the reaction of
both
cis
and
trans
stilbene with Br2
as part of your prelab procedure.
Note: I'm not sure what the
mechanisms look like so that's why I'm having trouble with the
products. Please, if you can, draw out the mechanisms for both of
these!! Thanks.
cis-stilbene trans-stilbene
Making sure to show all steps and arrows, draw a plausible
mechanism from the transformation shown below.
1) Making sure to show all steps and arrows, draw a plausible mechanism for the transformation shown below. (10 points) ОН - &- + HBr Br
Draw a plausible mechanism??? help please!
1) Making sure to show all steps and arrows, draw a plausible mechanism for the transformation show below. (10 points) + HBr
PART III. Mechanism problems 38. Please draw a plausible reaction mechanism of solvolysis reaction by showing poessbility of reermeer ned ntemesatws with the mao prmist. If there isa possibility of rearrangement, please show it for the major product CH3 39. Propose a detailed, step-by-step mechanism for the reaction pathway shown below. 40. CH,CH,CH,Br+NaCCC 41. Plcase draw a plausible reaction mechanism of the following free radical reaction by showing the initiation step, propagation step, and termination step. Bry
I need to know the mechanism for step 1- it should be
detailed showing all curved arrows and the correct molecular
structures for reactants, intermediates, and products. thank you
for your help!
2. Nitration and the Hofmann Rearrangement Monk, K.A.; Mohan R.S. The Hofmann Rearrangement Using Househo Synthesis of 3-Nitroaniline). Chem. Educ. 1999,76,1717 and McElveen, vardinas, K.; Stamberger, J.A.: Mohan. R.S. The Discovery-Oriented Approach Organic Chemistry 1. Nitration of Unknown Organic Compounds.). Chem. 1999, 76,535-536.) Step 1. Preparation of 3-nitrobenzamide...
Draw the Mechanism for the following reaction. Make sure to have correct stereochemistry and proper structure in all your structures. You may show just one sterosome throughout your mechanism, but provide all possibilities in your final answer
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