I have a table but while I was practicing with the other examples I notice that...
I have a table but while I was practicing with the other examples I notice that my table not always work... how can I know which reaction works better (SN1, SN2, E1, E2, E1cB)?
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I have a table but while I was practicing with the other
examples I notice that...
I am having trouble differing between Sn1, Sn2, E1, and E2 reactions. Please help me understand...
I am having trouble differing between Sn1, Sn2, E1, and E2
reactions. Please help me understand how to approach these
problems. I've attempted to answer them, but I am not confident in
my answers. Please show me how to get to the correct answer.
1. [is it A?]
2. [Is it C?]
3. [is it 3 and 4?]
A) I
B) II
C) III
D) IV
E) I and II
F) III and IV
Predict the mechanism (S\2, E2, SN1,...
Organic Chemistry: Vocabulary: i.) If we have a weakly basic nucleophile and a secondary haloalkane we’ll...
Organic Chemistry: Vocabulary: i.) If we have a weakly basic nucleophile and a secondary haloalkane we’ll generally get _ mechanism(s). a. SN1 only b. SN2 c. E2 d. E1 only e. SN1 and E1 f. no reaction This mechanism will have ____ stereochemistry, a. predictable b. random due to the ____. a. planar intermediate b. backside attack transition state c. frontside attack transition state d. anti-periplanar transition state _____________________________________________________ ii.) Carbocation rearrangements will tend to form the __ stable intermediate....
1) Compare and contrast SN1, SN2, E1, and E2 reactions! (similarities abd differences. Requirements for each...
1) Compare and contrast SN1, SN2, E1, and E2 reactions!
(similarities abd differences. Requirements for each to
work.)
2) Why is SN2 is in direct competition with E2 while SN1 is
direct competition with E1 reaction.
3) Rate expression of each
4) which reactions are concerted? Which are atep wise?
5) which are sterospecific and what stereospecificity of each
are?
6) how do the variables below (A-D) influence reaction
pathway?
Compare and contrast SNI, SN2, El and E2 reactions. What...
Compare and contrast SN1, SN2, E1 and E2 reactions. What are some obvious similarities and differences...
Compare and contrast SN1, SN2, E1 and E2 reactions. What are some obvious similarities and differences between each reaction pathway? What are the requirements for each reaction to work? Discuss why SN2 is in direct competition with E2 while SN1 is in direct competition with the E1 reaction pathway. What is the rate expression for each? Which reactions are concerted? Which reactions are step-wise? Which reactions are stereospecific and what is the stereospecificity of each that are? How do the...
I need help with B. Professor's answer is SN2 but I thought it was E2 25. Draw the major product(s) expected for eac...
I
need help with B. Professor's answer is SN2 but I thought it was E2
25. Draw the major product(s) expected for each reaction and also how each product is formed (options: SN1, SN2, E1, E2). Some reactions may occur via multiple pathways, in which case you should draw the major product for each pathway. Be sure to account for stereochemistry in your answers. If there is no reaction, write "No Reaction". Ez AL HACI 10 BuOK BuOH No SN...
Can you explain this in very much detail including background theory and things I have to...
Can you explain this in very much detail including background
theory and things I have to know to solve this?
The reaction below would go via: он о CN DMF PRODUCT(S) A. SN1 mechanism with inversion B. SN1 mechansim with racemic product C. SN2 mechanism with stereoretention D. SN2 mechanism with racemic product E. SN2 mechanism with inversion What is the product?
I don't know how to distinguish E1 and E2 reacions. For E2 reactions I have trouble...
I don't know how to distinguish E1 and E2 reacions.
For E2 reactions I have trouble with the transition state. These
reactions need intermediate steps and transition states but not
products.
1. (i) (2.5 points x 10-25 points) For the following elimination reactions Write bond-line structure of the substrate and the reagent Write full mechanism for the reaction transition state for E2, intermediate for El) and name the reaction either as El or E2; Write all possible products of the...
Why does Thevenin's Theorem work? I understand how to use it but I don't understand why...
Why does Thevenin's Theorem work? I understand how to use it but I don't understand why it works. I have been reading my textbook and can follow the procedure, but I want to understand on a deeper level why the author does what they do. So far I know that the steps are 1. Find Vth, the open terminal voltage 2. Find isc, the short circuit current Vth 3. Rth isc But I don't know why these steps work. I...
[Review Topics) (References) Give an IUPAC name for the compound below. Accepted names for branched alkyl...
[Review Topics) (References) Give an IUPAC name for the compound below. Accepted names for branched alkyl groups are isopropyl, isobutyl, sec-butyl, and tert-butyl. CH2CH3 CH3CH2CH2CCH2CH3 Submit Answer Retry Entire Group 9 more group attempts remaining The two reactants shown below are combined to bring about a nucleophilic substitution reaction. Br NaOCCH, . CH3CH2CHCH 1. none h. HBr 1.H20 e. "CCH3 f. Br j. Nat 9. HOCCH3 k. "OCCH3 Which letter designates the electrophilic carbon at which substitution occurs? (If no...
I am taking a business law class and we have to answer two questions regarding two...
I am taking a business law class and we have to answer two
questions regarding two hypothetical examples. I missed the class
examples and was hoping someone could help me with finding out the
most relevant cases to the question and how to approach answering
them. Thanks!
1. Queens College, recognizing that its black male students are in better physical shape than other students institutes a policy under which anyone not a black male needs to take 2 FNES classes...
I am having trouble differing between Sn1, Sn2, E1, and E2
reactions. Please help me understand how to approach these
problems. I've attempted to answer them, but I am not confident in
my answers. Please show me how to get to the correct answer.
1. [is it A?]
2. [Is it C?]
3. [is it 3 and 4?]
A) I
B) II
C) III
D) IV
E) I and II
F) III and IV
Predict the mechanism (S\2, E2, SN1,...
1) Compare and contrast SN1, SN2, E1, and E2 reactions!
(similarities abd differences. Requirements for each to
work.)
2) Why is SN2 is in direct competition with E2 while SN1 is
direct competition with E1 reaction.
3) Rate expression of each
4) which reactions are concerted? Which are atep wise?
5) which are sterospecific and what stereospecificity of each
are?
6) how do the variables below (A-D) influence reaction
pathway?
Compare and contrast SNI, SN2, El and E2 reactions. What...
I
need help with B. Professor's answer is SN2 but I thought it was E2
25. Draw the major product(s) expected for each reaction and also how each product is formed (options: SN1, SN2, E1, E2). Some reactions may occur via multiple pathways, in which case you should draw the major product for each pathway. Be sure to account for stereochemistry in your answers. If there is no reaction, write "No Reaction". Ez AL HACI 10 BuOK BuOH No SN...
Can you explain this in very much detail including background
theory and things I have to know to solve this?
The reaction below would go via: он о CN DMF PRODUCT(S) A. SN1 mechanism with inversion B. SN1 mechansim with racemic product C. SN2 mechanism with stereoretention D. SN2 mechanism with racemic product E. SN2 mechanism with inversion What is the product?
I don't know how to distinguish E1 and E2 reacions.
For E2 reactions I have trouble with the transition state. These
reactions need intermediate steps and transition states but not
products.
1. (i) (2.5 points x 10-25 points) For the following elimination reactions Write bond-line structure of the substrate and the reagent Write full mechanism for the reaction transition state for E2, intermediate for El) and name the reaction either as El or E2; Write all possible products of the...
Why does Thevenin's Theorem work? I understand how to use it but I don't understand why it works. I have been reading my textbook and can follow the procedure, but I want to understand on a deeper level why the author does what they do. So far I know that the steps are 1. Find Vth, the open terminal voltage 2. Find isc, the short circuit current Vth 3. Rth isc But I don't know why these steps work. I...
[Review Topics) (References) Give an IUPAC name for the compound below. Accepted names for branched alkyl groups are isopropyl, isobutyl, sec-butyl, and tert-butyl. CH2CH3 CH3CH2CH2CCH2CH3 Submit Answer Retry Entire Group 9 more group attempts remaining The two reactants shown below are combined to bring about a nucleophilic substitution reaction. Br NaOCCH, . CH3CH2CHCH 1. none h. HBr 1.H20 e. "CCH3 f. Br j. Nat 9. HOCCH3 k. "OCCH3 Which letter designates the electrophilic carbon at which substitution occurs? (If no...
I am taking a business law class and we have to answer two
questions regarding two hypothetical examples. I missed the class
examples and was hoping someone could help me with finding out the
most relevant cases to the question and how to approach answering
them. Thanks!
1. Queens College, recognizing that its black male students are in better physical shape than other students institutes a policy under which anyone not a black male needs to take 2 FNES classes...
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