Homework Answers
primary alkyl halides undergoes the SN2 reaction with
NaOCH3 / CH3OH and the secondary alkyl halide undergoes the SN1
mechanism with water i.e first carbo cation is formed and the
nucleophilic attack produces the product
Add Answer to:
Please show the mechanism showing all possible substitution
products. SN1 and SN2 only. Thank you.
Determine...
Only using E1 and E2 and please show mechanism. Thank you. Determine the major elimination product(s)...
Only using E1 and E2 and please show mechanism. Thank
you.
Determine the major elimination product(s) for each of the following reactions. addition, please state the mechanism that is employed in the formation product. (12 points) HO H2SO4 Br NaOC(CH3)3 CH3OH CH3OH Heat
please show all steps including each mechanism (arrows) and also if SN1 has any rearrangements of...
please show all steps including each mechanism (arrows) and
also if SN1 has any rearrangements of carbocation intermediate
through a hydride shift and/or methyl shift. DO NOT NEED
ELIMINATION. ONLY SUBSTITUTION.
Sy1/E1 versus S2/E2 Learning Checks Draw the major organic substitution and/or elimination products in the following reactions. If no reaction is possible, write “No Reaction". Substitution Product(s) Elimination Product(s) 2) 2) OH BrCH K* -Ot-Bu NaOCH н"Сн, сн,он нсн, Ph NaOCH Br H CH3OH CH NaOCH NaOH T.CH, I...
Determine the major substitution product(s) for each of the following reactions. In addition, please state the...
Determine the major substitution product(s) for each of the following reactions. In addition, please state the mechanism that is employed in the formation of each product. (8 points) Br NaOCH CH2OH Br Н,0. Heat
please do all and explain sn1 sn2 e1e2 1. Write a full, complete mechanism for each...
please do all and explain sn1 sn2 e1e2
1. Write a full, complete mechanism for each of the following reactions. Be sure to indicate all mechanism arrows, charges, and lone electrons. Show stereochemistry where appropriate. Do not show transition states. You must show all possible products, but you only have to write the full mechanism for the formation of one product. (15 points): Br: a) ~ Br H2O2 b) 0-5- NaOH NaOCH, 4.5 de the reaction mat occurs more quickly...
please explain in detail. Thank you in advance . 1. Circle the mechanism (SN2, SN1, E2,...
please explain in detail. Thank you in advance .
1. Circle the mechanism (SN2, SN1, E2, or E1) responsible for the formation of each product in this reaction. If the product cannot be formed in the reaction, circle "not a product". (2 pts) CI CHE CH3 CHE CH3 осна SN2 SN1 E2 E1 S2 SN1 E2 E1 SN2 Sn1 E2 E1 SN2 SN1 E2 E1 not a product not a product not a product not a product 2. These reactions...
major products formed by substitution (Sn1and Sn2) Answer all 4 questions for a total of 100 points. An additional...
major products formed by substitution (Sn1and Sn2)
Answer all 4 questions for a total of 100 points. An additional 8 points is given to the bonus question. 1a) Give the major product formed by the following substitution reactions: (3 points) by Give the major product formed by the following $2 substitution reaction and the mechanism for it formation: (6 points) Н. c) Give the major product formed by the following S1 substitution reactions and the mechanism for its formation: (16...
predict the mechanism (Sn1, Sn2, E1, E2) and major products for each reaction 8) NaOCHy CH,CHE...
predict the mechanism (Sn1, Sn2, E1, E2) and major products for
each reaction
8) NaOCHy CH,CHE CH,OH CH CH heat H,PO heat KOB HOIBU CHO CH, NaN. Br. H NaOCH CH3CH2OH heat dapted from Ruehl
5. Predict the major organic products of the following reactions. Show all asymmetric carbons with wedgeldash...
5. Predict the major organic products of the following reactions. Show all asymmetric carbons with wedgeldash notation (i.e., as shown in the starting material). If a reaction produces a racemic mixture, show only one of the enantiomers produced. Carefully note the requested reaction mechanism for each reaction. (20 pts) NaOCH3 CH3OH SN2 Br CH3OH SN1 Br NaOCH3 CH3OH E2 Show Zaitsev product Br CH3OH Br E1
For the following substitution reactions predict the products showing stereochemistry only if is of relevance. Also...
For the following substitution reactions predict the
products showing stereochemistry only if is of relevance. Also
comment on what type of reaction: Sn1 or Sn2. Finally is the
starting material and product optically active or inactive?
Explain.
CH3CH2CH3 НО HBr CH-Br НЫС
1.) Determine the mechanism. (Sn1 or Sn2) 2.) Show step by step reaction mechanism of nucleophilic...
1.) Determine the mechanism. (Sn1 or Sn2)
2.) Show step by step reaction mechanism of nucleophilic
substitution including transition states
3.) Draw the products, including stereochemistry
Br + CN acetone
Only using E1 and E2 and please show mechanism. Thank
you.
Determine the major elimination product(s) for each of the following reactions. addition, please state the mechanism that is employed in the formation product. (12 points) HO H2SO4 Br NaOC(CH3)3 CH3OH CH3OH Heat
please show all steps including each mechanism (arrows) and
also if SN1 has any rearrangements of carbocation intermediate
through a hydride shift and/or methyl shift. DO NOT NEED
ELIMINATION. ONLY SUBSTITUTION.
Sy1/E1 versus S2/E2 Learning Checks Draw the major organic substitution and/or elimination products in the following reactions. If no reaction is possible, write “No Reaction". Substitution Product(s) Elimination Product(s) 2) 2) OH BrCH K* -Ot-Bu NaOCH н"Сн, сн,он нсн, Ph NaOCH Br H CH3OH CH NaOCH NaOH T.CH, I...
Determine the major substitution product(s) for each of the following reactions. In addition, please state the mechanism that is employed in the formation of each product. (8 points) Br NaOCH CH2OH Br Н,0. Heat
please do all and explain sn1 sn2 e1e2
1. Write a full, complete mechanism for each of the following reactions. Be sure to indicate all mechanism arrows, charges, and lone electrons. Show stereochemistry where appropriate. Do not show transition states. You must show all possible products, but you only have to write the full mechanism for the formation of one product. (15 points): Br: a) ~ Br H2O2 b) 0-5- NaOH NaOCH, 4.5 de the reaction mat occurs more quickly...
please explain in detail. Thank you in advance .
1. Circle the mechanism (SN2, SN1, E2, or E1) responsible for the formation of each product in this reaction. If the product cannot be formed in the reaction, circle "not a product". (2 pts) CI CHE CH3 CHE CH3 осна SN2 SN1 E2 E1 S2 SN1 E2 E1 SN2 Sn1 E2 E1 SN2 SN1 E2 E1 not a product not a product not a product not a product 2. These reactions...
major products formed by substitution (Sn1and Sn2)
Answer all 4 questions for a total of 100 points. An additional 8 points is given to the bonus question. 1a) Give the major product formed by the following substitution reactions: (3 points) by Give the major product formed by the following $2 substitution reaction and the mechanism for it formation: (6 points) Н. c) Give the major product formed by the following S1 substitution reactions and the mechanism for its formation: (16...
predict the mechanism (Sn1, Sn2, E1, E2) and major products for
each reaction
8) NaOCHy CH,CHE CH,OH CH CH heat H,PO heat KOB HOIBU CHO CH, NaN. Br. H NaOCH CH3CH2OH heat dapted from Ruehl
5. Predict the major organic products of the following reactions. Show all asymmetric carbons with wedgeldash notation (i.e., as shown in the starting material). If a reaction produces a racemic mixture, show only one of the enantiomers produced. Carefully note the requested reaction mechanism for each reaction. (20 pts) NaOCH3 CH3OH SN2 Br CH3OH SN1 Br NaOCH3 CH3OH E2 Show Zaitsev product Br CH3OH Br E1
For the following substitution reactions predict the
products showing stereochemistry only if is of relevance. Also
comment on what type of reaction: Sn1 or Sn2. Finally is the
starting material and product optically active or inactive?
Explain.
CH3CH2CH3 НО HBr CH-Br НЫС
1.) Determine the mechanism. (Sn1 or Sn2)
2.) Show step by step reaction mechanism of nucleophilic
substitution including transition states
3.) Draw the products, including stereochemistry
Br + CN acetone
Most questions answered within 3 hours.
-
Write a program to solve the Josephus problem, with the following
modification:
Sample Input:
./a.out n...
asked 46 minutes ago -
At the start of a CD it is spinning at a rate of 525 rpm
(revolutions...
asked 1 hour ago -
4. Without doing any calculations, predict whether the observed
∆T would increase, decrease or remain the...
asked 2 hours ago -
Based on the range, which of the following sets of scores has
the greatest variability? 3,...
asked 3 hours ago -
Ripples in a pond travel at a velocity of 3 m/s with one peak
passing a...
asked 3 hours ago -
A man stands on the roof of a building of height 13.0 mm and
throws a...
asked 3 hours ago -
The extent to which assets are financed by borrowed funds and
other liabilities is indicated by:...
asked 4 hours ago -
Explain in detail
Germany is the fifth largest economy
explain what goods and services Germany specializes...
asked 4 hours ago -
The density of platinum is 21.45 g/mL. If a cube of platinum
with a mass of...
asked 5 hours ago -
Accounts Receivable
Sales
A/R Posting
Extended Sales Invoice
Packing Slip
Compare invoice to packing slip 2...
asked 5 hours ago -
Michaella, age 23, is a full-time law student and is claimed by
her parents as a...
asked 5 hours ago -
Why are polymers not typically casted into products?
asked 5 hours ago