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So I'm looking for some clarification on the products from
this rxn. I got two different...
I'm not sure if 4 is correct so I just wanted some clarification, and for 5...
I'm not sure if 4 is correct so I just wanted some
clarification, and for 5 I also am not sure as I need more
reasoning for why product B was formed!
4. Propose an arrow-pushing mechanism for the reaction below. 1. Cl₂, H₂O 2. NaH HO O-H Loh HOH Na-u 00 27, 5. During a “routine" bromination of an alkene, a team of researchers at the University of Georgia were surprised to find that got a significant amount of...
Please answer all two questions and please explain! I'm completely lost at the moment and I'm...
Please answer all two
questions and please explain! I'm completely lost at the moment and
I'm not sure how to solve it. Please do it step by step if
possible.
10. (10 points) Account for the relative product distribution for the radical bromination reaction shown below. (a) Write the hydrogen abstraction step reaction (radical formation), including the transition state, that leads to each product. (b) Match each reaction to the correct reaction coordinate diagram. Draw the reactants on the energy...
Draw the structure of the major organic product(s) of the reaction. I'm pretty sure I got...
Draw the structure of the major organic product(s) of the
reaction.
I'm pretty sure I got the answer right as it becomes a
carboxylic acid with a HCL byproduct but it's seen as wrong. Is it
the formatting or something?
Draw the structure of the major organic product(s) of the reaction. H20 CI You do not have to consider stereochemistry. All carboxyl and amino groups should be drawn in the neutral form. Draw one structure per sketcher. Add additional sketchers...
I just want to confirm that I did this correctly. I am drawing 2 products from...
I just want to confirm that I did this correctly. I am
drawing 2 products from the first present reagent. If it first
combines with H-Br, then H-Cl. Are my products correct and is it
correct that this is not a racemic mixture?
Also I forget to add the Br in the first product. Also
is the first product racemic??
PI Draw Product THBr (2) Нc| Prow Product i CI br are n105 different The SU product is not racemic...
So I got some questions left, I already calculated them and got some help from here,...
So I got some questions left, I already calculated them and got some help from here, but the results were wrong according to the evaluation system. Question 1: Use the table below, and calculate the Spearman rank correlation coefficient (hint: the rejection point is 0.6833, and thus, we reject the null hypothesis; thus we conclude that the x & y are correlated). x y 2.36 0.91 5.2 1.91 2.44 1.69 3.25 1.22 6.82 1.79 5.79 1.27 3.96 1.79 3.36 1.33...
CONTEXT So we did an Sn1 reaction in chem lab to convert t-butyl alcohol to t-butyl...
CONTEXT So we did an Sn1 reaction in chem lab to convert t-butyl alcohol to t-butyl chloride by the following reaction C4H10O + HCl --> C4H9Cl + H2O We did this by mixing the HCl and the t-butyl alcohol in a separatory funnel, then we collected the organic layer that formed and vacuum distilled the product. QUESTIONS What is something that could cause a low yield in this experiment? we got a 26% yield, I was thinking maybe heating up...
So I got some questions left, I already calculated them and got some help from here, but the results were wrong according to the evaluation system. Question 1: Use the table below, and calculate the S...
So I got some questions left, I already calculated them and got some help from here, but the results were wrong according to the evaluation system. Question 1: Use the table below, and calculate the Spearman rank correlation coefficient (hint: the rejection point is 0.6833, and thus, we reject the null hypothesis; thus we conclude that the x & y are correlated). x y 2.36 0.91 5.2 1.91 2.44 1.69 3.25 1.22 6.82 1.79 5.79 1.27 3.96 1.79 3.36 1.33...
Samsung's wearable strategy is two-pronged. It's got the mainstream wearables, like your Gear Sport and Gear...
Samsung's wearable strategy is two-pronged. It's got the mainstream wearables, like your Gear Sport and Gear Fit2 Pro, but it's also got a lot of experimentations in digital health. This is stuff that's way far down the line, but the company wants to show off anyway. The most famous example of this is the Samsung Simband. It was a reference wearable that was packed with sensors that could track blood pressure, skin temperature, sweat production, blood volume, heart rate, and...
If anyone could give me some guidance for these questions. I know i'm chancing my arm...
If anyone could give me some guidance for these questions. I know i'm chancing my arm but its worth a shot.... Thanks in advance i.Write a private instance method cycleState() which takes no argument and returns no value. This method cycles the value of state, from 1 to 2, from 2 to 3, from 3 to 4 and from 4 back to 1 again. (Note that the value of 0 for state is not part of this cycle). ii.Write a...
If anyone could give me some guidance for these questions. I know i'm chancing my arm but its worth a shot.... Thanks in advance i.Write a private instance method cycleState() which takes no ar...
If anyone could give me some guidance for these questions. I know i'm chancing my arm but its worth a shot.... Thanks in advance i.Write a private instance method cycleState() which takes no argument and returns no value. This method cycles the value of state, from 1 to 2, from 2 to 3, from 3 to 4 and from 4 back to 1 again. (Note that the value of 0 for state is not part of this cycle). ii.Write a...
I'm not sure if 4 is correct so I just wanted some
clarification, and for 5 I also am not sure as I need more
reasoning for why product B was formed!
4. Propose an arrow-pushing mechanism for the reaction below. 1. Cl₂, H₂O 2. NaH HO O-H Loh HOH Na-u 00 27, 5. During a “routine" bromination of an alkene, a team of researchers at the University of Georgia were surprised to find that got a significant amount of...
Please answer all two
questions and please explain! I'm completely lost at the moment and
I'm not sure how to solve it. Please do it step by step if
possible.
10. (10 points) Account for the relative product distribution for the radical bromination reaction shown below. (a) Write the hydrogen abstraction step reaction (radical formation), including the transition state, that leads to each product. (b) Match each reaction to the correct reaction coordinate diagram. Draw the reactants on the energy...
Draw the structure of the major organic product(s) of the
reaction.
I'm pretty sure I got the answer right as it becomes a
carboxylic acid with a HCL byproduct but it's seen as wrong. Is it
the formatting or something?
Draw the structure of the major organic product(s) of the reaction. H20 CI You do not have to consider stereochemistry. All carboxyl and amino groups should be drawn in the neutral form. Draw one structure per sketcher. Add additional sketchers...
I just want to confirm that I did this correctly. I am
drawing 2 products from the first present reagent. If it first
combines with H-Br, then H-Cl. Are my products correct and is it
correct that this is not a racemic mixture?
Also I forget to add the Br in the first product. Also
is the first product racemic??
PI Draw Product THBr (2) Нc| Prow Product i CI br are n105 different The SU product is not racemic...
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