Homework Answers
Add Answer to:
Please follow the instructions and complete!
1. (24pts) In the empty boxes, draw the structure of...
Draw the Major alkene product and minor where indicated. Show the correct alkene geometry and/or absolute...
Draw the Major alkene product and minor where indicated. Show
the correct alkene geometry and/or absolute configuration at carbon
stereocenters. (Follow side instructions as asked like on D and
E).
1. (24pts) In the empty boxes, draw the structure of the MAJOR alkene product expected following each E2 reaction. Where indicated, also draw the minor alkene(s) formed. Also, show the correct akene geometry and/or absolute configuration at carbon stereocenters present in any of the products expected. Follow any additional instruction...
Draw the bond line structural formulas for the products in the following reactions in the boxes...
Draw the bond line structural formulas for the products in the
following reactions in the boxes provided (one structure per box).
Where appropiate, clearly show stereochemistry.
[2] e) HBr major product minor product [1.51 ) КОН ethanol НС" Br HC HCI Be prepared to provide structural formula for the starting reactants if given products *** (1 h) 1) O3 2) Zn, H20, H* Но 0 1) O3 2) Zn, H202 0 + [2] 1) KMnO4 141 8. Provide the missing...
please answer all parts, thanks! 1. More substituted alkenes are more stable than less substituted alkenes....
please answer all parts, thanks!
1. More substituted alkenes are more stable than less substituted alkenes. Show the orbital overlap that helps to explain this observation. 2. Why is the heat of hydrogenation for an alkene exothermic? Analyze the bonds that are changing. AH = -30 kcal/mol Explain: + H2 3. Treating alkene "A" below with HBr can lead to a number of products. "A" SM + H-Br A bunch of products. For real, hella products. 3.A. Label the stereocenters...
8) Predict the product(s) of the following E2 reaction. Be sure to include solid wedges and...
8) Predict the product(s) of the following E2 reaction. Be sure to include solid wedges and dashed es on your product(s). Use conformational structures (the templates below) to show the mechanism and explain your reasoning Br CHCH ONa CH CH2OH, 70 °C Explanation(s): 9) Consider the E1 reaction of (3S)-3-bromo-2,3-dimethylpentane to form alkenes a) Draw the structure of the haloalkane (be sure to include stereochemistry). Clearly label any chiral carbon atoms with an asterisk ). b) Draw the structures of...
1. [10 pts] Consider the elimination reaction for the following alkyl halide with sodium methoxide in...
1. [10 pts] Consider the elimination reaction for the following alkyl halide with sodium methoxide in methanol (Na* OCH, CH,OH). CH NaOme MeOH CH Compound A Problem 2c Draw the major expected organic product (a) Redraw Compound A as seen in Viewpoint I below left as a Newman projection on the template provided in Problem 2a (below). Hint: Fill in missing Hs ar C2 and C3 to help you get started! (b) Rotate the C2 C3 bond to obtain the...
How do I answer questions in number 6 please, Thanks 6) (12 points) Draw mechanisms for...
How do I answer questions in number 6 please, Thanks
6) (12 points) Draw mechanisms for the following transformations +HC HO Br2 + HBr H3C H3 hv H3C rパ HO Br H2O + HBr c) (Hint for Se: Doubling the concentration of water has no effect on the rate.) 7.) (4 points) For the reaction in question 6b,t below is seen product, and what product ratio of question 6b is in fact the major prod stabilities of intermediates involved in...
(C) Protonation of alkene to form a carbocation followed by addition of bromide ion (D) Addition...
(C) Protonation of alkene to form a carbocation followed by addition of bromide ion (D) Addition of the proton to one face of the alkene with simultaneous delivery of a bromide ion from a different molecule of H-Br. 11. Which compound is the strongest nmucleophile for reaction of methane methanesulfonate (CHOS0.CH) in methanol at room temperature? (You may assume that everything is soluble in methanol) (A) potassium bromide (B) cesium iodide (C) sodiam chloride (D) lithium flaoride 12. Which proton...
Please complete for Tuesday, we will go through the questions and mark them in class. pg 156 - 4.23,...
Please complete for Tuesday, we will go through the questions and mark them in class. pg 156 - 4.23, 4.24, 4.26 pg 170 - 4.29, 4.31, pg 171-4.36 pg 175 - 4.59 pg 176- 4.74, 4.75, 4.80 pg 177-4.81, 4.82 pg 188- 5.1, 5.4, 5.5, 5.6, 5.11 - Using Table 5.1 pg 198-5.22, 5.25 pg 203 - 5.29 pg 206 - 5.37 pg 209 - 5.39 pg 2.14 5.61 pg 235-6.11, 6.14, 6.16 156 CHAPTER 4 Introduction to Organic Compounds...
Draw the Major alkene product and minor where indicated. Show
the correct alkene geometry and/or absolute configuration at carbon
stereocenters. (Follow side instructions as asked like on D and
E).
1. (24pts) In the empty boxes, draw the structure of the MAJOR alkene product expected following each E2 reaction. Where indicated, also draw the minor alkene(s) formed. Also, show the correct akene geometry and/or absolute configuration at carbon stereocenters present in any of the products expected. Follow any additional instruction...
Draw the bond line structural formulas for the products in the
following reactions in the boxes provided (one structure per box).
Where appropiate, clearly show stereochemistry.
[2] e) HBr major product minor product [1.51 ) КОН ethanol НС" Br HC HCI Be prepared to provide structural formula for the starting reactants if given products *** (1 h) 1) O3 2) Zn, H20, H* Но 0 1) O3 2) Zn, H202 0 + [2] 1) KMnO4 141 8. Provide the missing...
please answer all parts, thanks!
1. More substituted alkenes are more stable than less substituted alkenes. Show the orbital overlap that helps to explain this observation. 2. Why is the heat of hydrogenation for an alkene exothermic? Analyze the bonds that are changing. AH = -30 kcal/mol Explain: + H2 3. Treating alkene "A" below with HBr can lead to a number of products. "A" SM + H-Br A bunch of products. For real, hella products. 3.A. Label the stereocenters...
8) Predict the product(s) of the following E2 reaction. Be sure to include solid wedges and dashed es on your product(s). Use conformational structures (the templates below) to show the mechanism and explain your reasoning Br CHCH ONa CH CH2OH, 70 °C Explanation(s): 9) Consider the E1 reaction of (3S)-3-bromo-2,3-dimethylpentane to form alkenes a) Draw the structure of the haloalkane (be sure to include stereochemistry). Clearly label any chiral carbon atoms with an asterisk ). b) Draw the structures of...
1. [10 pts] Consider the elimination reaction for the following alkyl halide with sodium methoxide in methanol (Na* OCH, CH,OH). CH NaOme MeOH CH Compound A Problem 2c Draw the major expected organic product (a) Redraw Compound A as seen in Viewpoint I below left as a Newman projection on the template provided in Problem 2a (below). Hint: Fill in missing Hs ar C2 and C3 to help you get started! (b) Rotate the C2 C3 bond to obtain the...
How do I answer questions in number 6 please, Thanks
6) (12 points) Draw mechanisms for the following transformations +HC HO Br2 + HBr H3C H3 hv H3C rパ HO Br H2O + HBr c) (Hint for Se: Doubling the concentration of water has no effect on the rate.) 7.) (4 points) For the reaction in question 6b,t below is seen product, and what product ratio of question 6b is in fact the major prod stabilities of intermediates involved in...
(C) Protonation of alkene to form a carbocation followed by addition of bromide ion (D) Addition of the proton to one face of the alkene with simultaneous delivery of a bromide ion from a different molecule of H-Br. 11. Which compound is the strongest nmucleophile for reaction of methane methanesulfonate (CHOS0.CH) in methanol at room temperature? (You may assume that everything is soluble in methanol) (A) potassium bromide (B) cesium iodide (C) sodiam chloride (D) lithium flaoride 12. Which proton...
Please complete for Tuesday, we will go through the questions and mark them in class. pg 156 - 4.23, 4.24, 4.26 pg 170 - 4.29, 4.31, pg 171-4.36 pg 175 - 4.59 pg 176- 4.74, 4.75, 4.80 pg 177-4.81, 4.82 pg 188- 5.1, 5.4, 5.5, 5.6, 5.11 - Using Table 5.1 pg 198-5.22, 5.25 pg 203 - 5.29 pg 206 - 5.37 pg 209 - 5.39 pg 2.14 5.61 pg 235-6.11, 6.14, 6.16 156 CHAPTER 4 Introduction to Organic Compounds...
Most questions answered within 3 hours.
-
Population Standard Deviation
5.0000
Sample Size
11
Sample Mean
54.9091
Confidence Interval
Confidence Coefficient
0.98
Lower...
asked 16 minutes ago -
Consider a t distribution with 15 degrees of freedom. Compute
P(-1.42<t<1.42). Round your answer to at...
asked 17 minutes ago -
2-chloro-2-methylpropane is classified as a ____.
primary alkyl chloride
secondary alkyl chloride
tertiary alkyl chloride
asked 15 minutes ago -
Help would be greatly appreciated
Mark each of the statements below as True (T) or False...
asked 17 minutes ago -
How the process improvement(poka-yoke, kaizen, deming cycle,
mistake-proofing, DMAIC) people can employ in their work or...
asked 19 minutes ago -
Write a program to control a bread machine. Allow the user to
input the type of...
asked 27 minutes ago -
Turn design in research is an examination of:
Question 5 options:
A)
What and how something...
asked 32 minutes ago -
A particle with a net charge of 1.2 mC is placed in a uniform
electric field...
asked 42 minutes ago -
For questions 1 and 2 below, using what you
have learned in class, analyze and discuss...
asked 42 minutes ago -
Zinc sulfide reacts with oxygen according to the reaction:
2ZnS(s)+3O2(g)→2ZnO(s)+2SO2(g) A reaction mixture initially
contains 3.4...
asked 48 minutes ago -
Using traditional
methods, it takes 9.0 hours to receive a basic flying license. A
new license...
asked 51 minutes ago -
The EPA wants to test a randomly selected sample of n
n
water specimens and estimate...
asked 58 minutes ago