Could someone show me how to do this:
Homework Answers
Optiton C is correct
Explanation: chlorination of alkane in presence of light involves free radical mechanism. Tertiary free radical is more stable so the halide ion goes and attacks at tertiary carbon atom. so the product is structure C.
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Could someone show me how to do this:
Predict the major product(s) in the radical-chain monochlorination...
2. The following is a radical chain reaction. Br. heat a. Which product is the major...
2. The following is a radical chain reaction. Br. heat a. Which product is the major product? (3 pts) b. Show two propagation steps for the formation of the major product. (6 pts) c. Explain, with intermediates, how the major product becomes the major. (6 pts) d. Explain, with TS, how the major product becomes the major. (6 pts)
Given the resonance structures of this radical intermediate, which do you predict is the major product...
Given the resonance structures of this radical intermediate, which do you predict is the major product of radical bromination? C) 50:50 mixture of the above two products
Can someone explain this to me and show me how to do the work. 7. Identify...
Can someone explain this to me and show me how to do the
work.
7. Identify the major product(s) in the reaction of (R)-2-bromopentane with sodium cyanide in DMSO? A. (R)-2-cyanopentane (S)-2-cyanopentane racemic mixture of 2-cyanopentane trans-2-pentene
if someone could show me how to do these problems it would be very helpful. Orate...
if someone could show me how to do these problems it would be
very helpful.
Orate the major products) or pronde the reagents for each reachan below lise bold and dashed wedges to show the proper stereochemistry where necessary Write both the O- and p- products where necessary (3pts each answer). Br (A) NILE NBS Kinenc Product Thermodynamio Product CHCH3 X CH₂ CH3 Na liquid Nitz (E) HO CH-C-CHE 0 etts CHg thay chci AlC3 hsou (G) NO₂ Chzical AlCl3...
draw all the possible monochlorination products that could possibly be formed upon radical chlorination of 2-methylpentane....
draw all the possible monochlorination products that could possibly be formed upon radical chlorination of 2-methylpentane. Highlight the product you believe would be formed in greatest quantity. **i was able to draw 6, but i feel they may be wrong - 3-chloro-2-methylpentane, 2-chloro-4-methylpentane, 1-chloro-4-methyl, 2,3,3-dimethylchloropentane, 2,2-chloromethylpentane, 2-chloromethylpentane**
how many different products are formed by the free radical monochlorination of racemic 2-bromobutane at the...
how many different products are formed by the free radical monochlorination of racemic 2-bromobutane at the bumber 3 carbon to give 2-bromo-3- chlorobutane? count enantiomers as two different products
if you could show how to do this radical mechanism that would be helpful
if you could show how to do
this radical mechanism that would be helpful
1) Predict the major product in each of the following transformations. Show the mechanism. 2) Show...
1) Predict the major product in each of the following
transformations. Show the mechanism.
2) Show how you could synthesize the products below using a
Grignard reagent and appropriate electrophile by drawing the
overall balanced equation. Include the mechanism.
Predict the major product in each of the following transformations. No mechanisms are required for this question. [3 Marks] 1. CH,сн,МgBr (еxcess) 2. HС{aq) 1. PhMgBr (1 equiv.) 2. HCI(aq) ОН HO 1. CH2MgBr (2 equiv.) 2. HCl(aq) Н Show how...
3. Predict the major product(s) for the following reactions. Show the stereochemistry of the product(s) when...
3. Predict the major product(s) for the following reactions. Show the stereochemistry of the product(s) when applicable. (a) (e) Br2, H20 H2 PL (1) Os04 (2) NaHSO4, H20 (1) 03 (2) DMS (1) CH2CO3H (2) H30*
[01] Give all three termination steps (using structures) for a radical chain reaction monochlorination (Clh/hv) of...
[01] Give all three termination steps (using structures) for a radical chain reaction monochlorination (Clh/hv) of cyclopropane to give chlorocyclopropane 1. 2. [01] a. Give the resulting structure from the following electron flow. b. Give the curved arrows on structure at left to indicate the electron flow in going to the resonance structure on the right. Be precise. 3. [O1] Give the structure of the major product for the following reaction as well as the two allylic resonance structures from...
2. The following is a radical chain reaction. Br. heat a. Which product is the major product? (3 pts) b. Show two propagation steps for the formation of the major product. (6 pts) c. Explain, with intermediates, how the major product becomes the major. (6 pts) d. Explain, with TS, how the major product becomes the major. (6 pts)
Given the resonance structures of this radical intermediate, which do you predict is the major product of radical bromination? C) 50:50 mixture of the above two products
Can someone explain this to me and show me how to do the
work.
7. Identify the major product(s) in the reaction of (R)-2-bromopentane with sodium cyanide in DMSO? A. (R)-2-cyanopentane (S)-2-cyanopentane racemic mixture of 2-cyanopentane trans-2-pentene
if someone could show me how to do these problems it would be
very helpful.
Orate the major products) or pronde the reagents for each reachan below lise bold and dashed wedges to show the proper stereochemistry where necessary Write both the O- and p- products where necessary (3pts each answer). Br (A) NILE NBS Kinenc Product Thermodynamio Product CHCH3 X CH₂ CH3 Na liquid Nitz (E) HO CH-C-CHE 0 etts CHg thay chci AlC3 hsou (G) NO₂ Chzical AlCl3...
if you could show how to do
this radical mechanism that would be helpful
1) Predict the major product in each of the following
transformations. Show the mechanism.
2) Show how you could synthesize the products below using a
Grignard reagent and appropriate electrophile by drawing the
overall balanced equation. Include the mechanism.
Predict the major product in each of the following transformations. No mechanisms are required for this question. [3 Marks] 1. CH,сн,МgBr (еxcess) 2. HС{aq) 1. PhMgBr (1 equiv.) 2. HCI(aq) ОН HO 1. CH2MgBr (2 equiv.) 2. HCl(aq) Н Show how...
3. Predict the major product(s) for the following reactions. Show the stereochemistry of the product(s) when applicable. (a) (e) Br2, H20 H2 PL (1) Os04 (2) NaHSO4, H20 (1) 03 (2) DMS (1) CH2CO3H (2) H30*
[01] Give all three termination steps (using structures) for a radical chain reaction monochlorination (Clh/hv) of cyclopropane to give chlorocyclopropane 1. 2. [01] a. Give the resulting structure from the following electron flow. b. Give the curved arrows on structure at left to indicate the electron flow in going to the resonance structure on the right. Be precise. 3. [O1] Give the structure of the major product for the following reaction as well as the two allylic resonance structures from...
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