Homework Answers
The detail answer with explaination is shown below.
Add Answer to:
please respond in neat handwriting or type detailing the
answers for 7 and its parts, thank...
please respond in neat handwriting or type detailing the answers for 7 and its parts, thank...
please respond in neat handwriting or type detailing the answers
for 7 and its parts, thank you
13. Rate data for the following substitution reaction are presented in the accompanying table. R-L + Nuc→ R-Nuc + L Based on the rate data below, does the substitution reaction above follow an Syl mechanism or an mechanism? SN Trial # (R-L] Nuc" Initial Rate (M/s) 0.1 M 0.1 M 3.1 x 10 2 0.1 M 6.2 x 10 3 0.2 M 0.2...
please respond in neat handwriting or type detailing the answers for 7 and its parts, thank...
please respond in neat handwriting or type detailing the
answers for 7 and its parts, thank you
7. The pk, of a typical ketone is 20. =O H₂C CH₂ F3 C CH₃ 84 1-3C CH3 R a. Draw the conjugate base of each compound. Will the pk, of the trifluoroketone be higher or lower? Justify your answer in terms of conjugate base stability. I low? Triflurokeeone will be alshor because the base. Is morestable (F) Mor electronegative. C
Thank you so much! (2 pts) Draw the major elimination products and Identify the mechanism responsible...
Thank you so much!
(2 pts) Draw the major elimination products and Identify the mechanism responsible (E1 or E2). If both E and Z isomers form, only draw the E alkene. If only one isomer forms, label the alkene "E,""Z," or neither 1. NaOCH3 а. Br НОСHЗ b. НОСНЗ C. CI NaOCH3 d. (6 pts) Draw the substitution and/or elimination product(s) for the following reactions and identify 2. the mechanism responsible (SN1, SN2, E1, or E2) for each product drawn....
Quickly show all steps and answers all parts of the question please thank you 3. In...
Quickly show all steps and
answers all parts of the question please thank you
3. In the deuterium-labeled compound below predict the product(s) of the elimination reaction of the following elimination reaction and tell whether the alkene formed contains deuterium or not. (20 pts) HCCH; OH H2SO4(aq) heat н,с (ii) NaOCH.CH CH,CH,OH heat CH3 (iii) Write a detail mechanism for the formation of the product in question 3(i).
Please type or neat handwriting Thank you 4. Two blocks of mass 3.00 kg and 5.00...
Please type or neat handwriting
Thank you
4. Two blocks of mass 3.00 kg and 5.00 kg are connected as shown to a spring k 25.0 N/m) that has one end fixed to a wall. The horizontal surface has a ukinetic) 0.35 and the pulley is frictionless. The 3.0 kg block will not leave the platform. The pulley is mass less. The system is released from rest with the spring unstretched A. What is the combined kinetic energy of the...
please explain in detail . thank you in advance . 3. (a) Draw both chair conformations...
please explain in detail . thank you in advance .
3. (a) Draw both chair conformations for (1R,2R4S)-4-t-butyl-1-chloro-2-ethylcyclohexane. Label the B-carbons (as Br, B2, etc.) in each chair structure; include all hydrogens on the B-carbons. (2.5 pts) nC (1R,2R 4S)-4-t-butyl-1-chloro- 2-ethylcyclohexane (b) Draw a square around the chair conformation most likely to undergo an E2 reaction and explain your choice. (1 pt) (c) Draw the major organic product (including stereochemistry) of the E2 reaction between (1R,2R 4S)-4-t-butyl-1-chloro-2-ethylcyclohexane and sodium ethoxide...
Please make it easy to read (no cursive) THANK YOU SO MUCH :) 7. Is it...
Please make it easy to read (no cursive) THANK YOU SO MUCH :)
7. Is it possible to tell if the following reaction took place via an E, or an E2 reaction? Explain why? H CH, H H Н. Base ΠΗ X + CH Br H 8. What is the majority product from the following Ez reaction, why? Br 9. Describe all of the reaction conditions necessary to complete the following reaction. Draw the mechanism. Оснэ
Please answer both parts. Thank you :) 5. (a) Convert Compound A (shown below) to its...
Please answer both parts. Thank you :)
5. (a) Convert Compound A (shown below) to its chair-like structure by placing the substituents of this compound in their proper location and orientation in the decalin skeleton. (3pts for correct structure) CH3 HO CH₂ decalin skeleton (needs completed) Compound A (b) (i) is the decalin skeleton shown above the cis or trans-decalin stereoisomer? (ii) Is this decalin ring able to undergo a chair-flip? (iii) Explain in two or less sentences why or...
Please completely answer the questions, thank you! For the reactions below, 1. supply the reagents needed...
Please completely answer the questions, thank you!
For the reactions below, 1. supply the reagents needed to carry out the reaction, by writing them above the reaction arrow. 2. Use choices 1A through 11, 2A through 24, and 3A through 3X, above to answer the questions about reaction types and mechanistic details. 3. For the reactions in column 3, that require you to diagram the mechanism, diagram the mechanism. Column 1 Column 2 Column 3 Type of Reaction The Reason...
all 3 questions please. thank you in advance!! Question 8: Draw the Syl and El products...
all 3 questions please. thank you in advance!!
Question 8: Draw the Syl and El products formed in the reaction of (CH3)3CBr with H,0. Show mechanism using arrows." CH3 CH3-C-Br + CH H-O-H Question 9: Draw the major E2 elimination product formed from the following: alkyl halide. Question 10: Give structures corresponding to each name. a)-7,7-dimethyl-4-octanol b)>5-methyl-4-propyl-3-heptanol" c)-2-tert-butyl-3-methylcyclohexanolº d)- trans-1,2-cyclohexanediol"
please respond in neat handwriting or type detailing the answers
for 7 and its parts, thank you
13. Rate data for the following substitution reaction are presented in the accompanying table. R-L + Nuc→ R-Nuc + L Based on the rate data below, does the substitution reaction above follow an Syl mechanism or an mechanism? SN Trial # (R-L] Nuc" Initial Rate (M/s) 0.1 M 0.1 M 3.1 x 10 2 0.1 M 6.2 x 10 3 0.2 M 0.2...
please respond in neat handwriting or type detailing the
answers for 7 and its parts, thank you
7. The pk, of a typical ketone is 20. =O H₂C CH₂ F3 C CH₃ 84 1-3C CH3 R a. Draw the conjugate base of each compound. Will the pk, of the trifluoroketone be higher or lower? Justify your answer in terms of conjugate base stability. I low? Triflurokeeone will be alshor because the base. Is morestable (F) Mor electronegative. C
Thank you so much!
(2 pts) Draw the major elimination products and Identify the mechanism responsible (E1 or E2). If both E and Z isomers form, only draw the E alkene. If only one isomer forms, label the alkene "E,""Z," or neither 1. NaOCH3 а. Br НОСHЗ b. НОСНЗ C. CI NaOCH3 d. (6 pts) Draw the substitution and/or elimination product(s) for the following reactions and identify 2. the mechanism responsible (SN1, SN2, E1, or E2) for each product drawn....
Quickly show all steps and
answers all parts of the question please thank you
3. In the deuterium-labeled compound below predict the product(s) of the elimination reaction of the following elimination reaction and tell whether the alkene formed contains deuterium or not. (20 pts) HCCH; OH H2SO4(aq) heat н,с (ii) NaOCH.CH CH,CH,OH heat CH3 (iii) Write a detail mechanism for the formation of the product in question 3(i).
Please type or neat handwriting
Thank you
4. Two blocks of mass 3.00 kg and 5.00 kg are connected as shown to a spring k 25.0 N/m) that has one end fixed to a wall. The horizontal surface has a ukinetic) 0.35 and the pulley is frictionless. The 3.0 kg block will not leave the platform. The pulley is mass less. The system is released from rest with the spring unstretched A. What is the combined kinetic energy of the...
please explain in detail . thank you in advance .
3. (a) Draw both chair conformations for (1R,2R4S)-4-t-butyl-1-chloro-2-ethylcyclohexane. Label the B-carbons (as Br, B2, etc.) in each chair structure; include all hydrogens on the B-carbons. (2.5 pts) nC (1R,2R 4S)-4-t-butyl-1-chloro- 2-ethylcyclohexane (b) Draw a square around the chair conformation most likely to undergo an E2 reaction and explain your choice. (1 pt) (c) Draw the major organic product (including stereochemistry) of the E2 reaction between (1R,2R 4S)-4-t-butyl-1-chloro-2-ethylcyclohexane and sodium ethoxide...
Please make it easy to read (no cursive) THANK YOU SO MUCH :)
7. Is it possible to tell if the following reaction took place via an E, or an E2 reaction? Explain why? H CH, H H Н. Base ΠΗ X + CH Br H 8. What is the majority product from the following Ez reaction, why? Br 9. Describe all of the reaction conditions necessary to complete the following reaction. Draw the mechanism. Оснэ
Please answer both parts. Thank you :)
5. (a) Convert Compound A (shown below) to its chair-like structure by placing the substituents of this compound in their proper location and orientation in the decalin skeleton. (3pts for correct structure) CH3 HO CH₂ decalin skeleton (needs completed) Compound A (b) (i) is the decalin skeleton shown above the cis or trans-decalin stereoisomer? (ii) Is this decalin ring able to undergo a chair-flip? (iii) Explain in two or less sentences why or...
Please completely answer the questions, thank you!
For the reactions below, 1. supply the reagents needed to carry out the reaction, by writing them above the reaction arrow. 2. Use choices 1A through 11, 2A through 24, and 3A through 3X, above to answer the questions about reaction types and mechanistic details. 3. For the reactions in column 3, that require you to diagram the mechanism, diagram the mechanism. Column 1 Column 2 Column 3 Type of Reaction The Reason...
all 3 questions please. thank you in advance!!
Question 8: Draw the Syl and El products formed in the reaction of (CH3)3CBr with H,0. Show mechanism using arrows." CH3 CH3-C-Br + CH H-O-H Question 9: Draw the major E2 elimination product formed from the following: alkyl halide. Question 10: Give structures corresponding to each name. a)-7,7-dimethyl-4-octanol b)>5-methyl-4-propyl-3-heptanol" c)-2-tert-butyl-3-methylcyclohexanolº d)- trans-1,2-cyclohexanediol"
Most questions answered within 3 hours.
-
Suppose that on a temperature scale X, water boils at 203.0°X
and freezes at -105.7°X. What...
asked 41 minutes ago -
BaS crystallizes in a cubic unit cell with S2- ions on each
corner and each face....
asked 1 hour ago -
A. 0≤P(Oi)≤10≤P(Oi)≤1 for each i
B. P(Oi)≤0P(Oi)≤0
C. P(Oi)=1+P(OCi)P(Oi)=1+P(OiC)
D. P(Oi)≥1P(Oi)≥1
If an experiment consists of...
asked 2 hours ago -
A battery has an emf of 9.20V and an internal resistance of 1.20
ohm. a)What resistance...
asked 2 hours ago -
The area of an elastic circular loop decreases at a constant
rate, dA/dt = −6.60×10−3 m2/s...
asked 3 hours ago -
The denaturation of proteins can be described by the
equilibrium
F⇌U
where F and U represent...
asked 5 hours ago -
Please answer what the maximum and minimum force is, and the
angle on the ion is...
asked 5 hours ago -
implement a program that reads a number of rows and a symbol.
The program will draw...
asked 5 hours ago -
Assume that when adults with smartphones are randomly selected,
45% use them in meetings or classes....
asked 5 hours ago -
Determine the number of formula units of
Na2SO4 and moles of oxygen contained in 8.11
moles...
asked 5 hours ago -
Explain in steps on the following code
What would be the output when executed
using System;...
asked 5 hours ago -
Given the information in the table, which of the following
statements is CORRECT?
Stock A
Stock...
asked 5 hours ago