Consider the reactivity of the cyclohexadienone derivative 8 to
address the questions below.
a. Predict the product of the following reaction.
b. Do you expect that the product of the reaction will be optically
active? Why or whynot?
Please help with Part B of this problem in organic chemistry.
Homework Answers
Add Answer to:
Consider the reactivity of the cyclohexadienone derivative 8 to address the questions below. a. Predict the...
The question is about E1,E2 reaction of organic chemistry. If a product is chiral, be sure...
The question is about E1,E2 reaction of organic chemistry. If a
product is chiral, be sure to label it as optically active or
racemic.
Predict the major deuterium containing product(s). If a product is chiral, be sure to label it as optically active or racemic. A. 1.) NaH он D3c 2.) Br Br В. KOTBU D3C racemic С. Br КОE+ D3C racemic D. NaN3 Br CD3
answer all questions 7. Draw and compare the free-energy diagram (potential energy curve) for the E1...
answer all questions
7. Draw and compare the free-energy diagram (potential energy curve) for the E1 and E2 reactions for a generic reaction shown below (LG-leaving group). Include all transition states and intermediates. E1 E E rxn coord. rxn coord. 8. For the following 2 substitution reactions, label the nucleophile, substrate, and leaving group. CH30CH2CH3 + Nal a) CH31+ CH3CH2ONA (CH3) 3 COCH3 + CH30H2 + Cl- b) 2CH30H+(CH3)3CCI 9 For each of the following pair of reactions, circle which...
please explain the work for both questions please 1. Predict the major organic product for each...
please explain the work for both questions please
1. Predict the major organic product for each of the following elimination reactions, and indicate whether each one occurs via the E1 or the E2 mechanism. Be sure to clearly indicate the proper stereochemical relationships between groups (if appropriate), and write the word “racemic” under any compound that is formed as a racemic mixture. Br AgNO3 H2O KOt-Bu H3CCH3 H36Br t-BuOH OTS NaOCH3 CH3OH CH3 NaOH H20 2. Draw all possible E2...
organic chemistry help! 1) for each reaction give the expected product 2) consider the conjugate bases,...
organic chemistry help!
1) for each reaction give the expected product
2) consider the conjugate bases, then arrange in order of
weakest to strongest
1. For each reaction give the expected product. 1. N(CH3)3 2. CICH,CH(CH3)2 CH3MgBr a) HO 1. KMnO4 2.SOCI2 d) CH 1. NaCN, DMSO (solvent) 2. LiAIHA 3. H₂O 2. Consider the conjugate bases of each of the following weak acids, then arrange the acids in order of weakest to strongest CI OH он OH
can someone please help me with this page??? thanks in advance!! 4. Predict the products for...
can someone please help me with this page??? thanks in
advance!!
4. Predict the products for the following reaction sequences. Он sOc/2 1. LIAIH 2. Hо (CH3)2NH (a) pyridine CH3Br base (-HBr) CH3CH2Br base (-HBr) (b) NH2 Br NaN3 (a) LIAIH (c) (b) Н-О MCРВА NaN3 (a) LIAIH4 (d) oH(a) NH2 NaBH3CN (e) H2SO4 5. Predict the major product for the following reactions. 1. excess CH3 NH2 (a) 2. Ag O, H2O heat 1. excess CH (b) 2. Ag20, H2O...
2. Not only does an aromatic ring itself affect the reactivity of an acid derivative (an ester, o...
2. Not only does an aromatic ring itself affect the reactivity of an acid derivative (an ester, on last year's quiz), substituents on the aromatic ring can further modify the reactivity. First, we will consider a phenyl amide with a para-acetyl substituent: CH, (a) What is the n-effect (resonance) of the para-acetyl substituent? How will that affect the reactivity of the other (amide) carbonyl in the molecule below (increase or decrease, compared to the same amide but with no p-...
Chemistry Organic 1 C306 01 Assignment 05, spring 2019 Answer All Questions. Consider the followi...
Chemistry Organic 1 C306 01 Assignment 05, spring 2019 Answer All Questions. Consider the following pairs of structures. Identify the relationship between them by 1. describing them as representing enantiomers, diastereomers, constitutional isomers, or two molecules of the same compound. CH3 CH3 a. HBr and Br CH3 b. and BrH H Br CH3 C. Br and CH3 CH3 d. Br СНу and CH3 CH3 e. Br an CH3 f. CH3 CH3 Brand H CH3 We were unable to transcribe this...
Organic Chemistry predict the product of the 8 alkyne reaction show. Hint: some may be used...
Organic Chemistry
predict the product of the 8 alkyne reaction show. Hint: some
may be used more than once and some may not be used at all.
Mix and Match Warning: Some answrers used more than once and some not at all! 1. H-CEC- H-Br (1 equiv) H-Br (s) 2. H-CEC- CL-Cl (1 equiv) 3. H-CEC- | Cl-CI (x3) 4. H-CEC- 5. H-CECH BE 6. H-CEC- 1) RBH (1 equiv) 2) KOH/H,02 1) RzBH (X 2) KOH/H,022 H,SO H2O(+ equiv)...
Below are two reactions, and one will occur faster than the other. Ts NaCN DMSO CH3...
Below are two reactions, and one will occur faster than the other. Ts NaCN DMSO CH3 Reaction A Ts NaCN H20 CH Reaction B Draw the major organic product for the reaction that will occur the fastest. Do not draw byproducts. C N S F H,N P "сн, Br
Please help me with the following organic chemistry chapter 7 questions. I keep getting them wrong...
Please help me with the following organic chemistry chapter 7
questions. I keep getting them wrong and I don't know why.
Draw a structural formula for the major organic product of the reaction shown. CH3CH2CH2CH2CH3 + нан HI Draw a structural formula for the major organic product of the reaction shown. CH3 [ CH3 + HCI → Draw a structural formula for the more stable carbocation intermediate formed in the reaction shown. HOD. + HI H3C
The question is about E1,E2 reaction of organic chemistry. If a
product is chiral, be sure to label it as optically active or
racemic.
Predict the major deuterium containing product(s). If a product is chiral, be sure to label it as optically active or racemic. A. 1.) NaH он D3c 2.) Br Br В. KOTBU D3C racemic С. Br КОE+ D3C racemic D. NaN3 Br CD3
answer all questions
7. Draw and compare the free-energy diagram (potential energy curve) for the E1 and E2 reactions for a generic reaction shown below (LG-leaving group). Include all transition states and intermediates. E1 E E rxn coord. rxn coord. 8. For the following 2 substitution reactions, label the nucleophile, substrate, and leaving group. CH30CH2CH3 + Nal a) CH31+ CH3CH2ONA (CH3) 3 COCH3 + CH30H2 + Cl- b) 2CH30H+(CH3)3CCI 9 For each of the following pair of reactions, circle which...
please explain the work for both questions please
1. Predict the major organic product for each of the following elimination reactions, and indicate whether each one occurs via the E1 or the E2 mechanism. Be sure to clearly indicate the proper stereochemical relationships between groups (if appropriate), and write the word “racemic” under any compound that is formed as a racemic mixture. Br AgNO3 H2O KOt-Bu H3CCH3 H36Br t-BuOH OTS NaOCH3 CH3OH CH3 NaOH H20 2. Draw all possible E2...
organic chemistry help!
1) for each reaction give the expected product
2) consider the conjugate bases, then arrange in order of
weakest to strongest
1. For each reaction give the expected product. 1. N(CH3)3 2. CICH,CH(CH3)2 CH3MgBr a) HO 1. KMnO4 2.SOCI2 d) CH 1. NaCN, DMSO (solvent) 2. LiAIHA 3. H₂O 2. Consider the conjugate bases of each of the following weak acids, then arrange the acids in order of weakest to strongest CI OH он OH
can someone please help me with this page??? thanks in
advance!!
4. Predict the products for the following reaction sequences. Он sOc/2 1. LIAIH 2. Hо (CH3)2NH (a) pyridine CH3Br base (-HBr) CH3CH2Br base (-HBr) (b) NH2 Br NaN3 (a) LIAIH (c) (b) Н-О MCРВА NaN3 (a) LIAIH4 (d) oH(a) NH2 NaBH3CN (e) H2SO4 5. Predict the major product for the following reactions. 1. excess CH3 NH2 (a) 2. Ag O, H2O heat 1. excess CH (b) 2. Ag20, H2O...
2. Not only does an aromatic ring itself affect the reactivity of an acid derivative (an ester, on last year's quiz), substituents on the aromatic ring can further modify the reactivity. First, we will consider a phenyl amide with a para-acetyl substituent: CH, (a) What is the n-effect (resonance) of the para-acetyl substituent? How will that affect the reactivity of the other (amide) carbonyl in the molecule below (increase or decrease, compared to the same amide but with no p-...
Chemistry Organic 1 C306 01 Assignment 05, spring 2019 Answer All Questions. Consider the following pairs of structures. Identify the relationship between them by 1. describing them as representing enantiomers, diastereomers, constitutional isomers, or two molecules of the same compound. CH3 CH3 a. HBr and Br CH3 b. and BrH H Br CH3 C. Br and CH3 CH3 d. Br СНу and CH3 CH3 e. Br an CH3 f. CH3 CH3 Brand H CH3 We were unable to transcribe this...
Organic Chemistry
predict the product of the 8 alkyne reaction show. Hint: some
may be used more than once and some may not be used at all.
Mix and Match Warning: Some answrers used more than once and some not at all! 1. H-CEC- H-Br (1 equiv) H-Br (s) 2. H-CEC- CL-Cl (1 equiv) 3. H-CEC- | Cl-CI (x3) 4. H-CEC- 5. H-CECH BE 6. H-CEC- 1) RBH (1 equiv) 2) KOH/H,02 1) RzBH (X 2) KOH/H,022 H,SO H2O(+ equiv)...
Below are two reactions, and one will occur faster than the other. Ts NaCN DMSO CH3 Reaction A Ts NaCN H20 CH Reaction B Draw the major organic product for the reaction that will occur the fastest. Do not draw byproducts. C N S F H,N P "сн, Br
Please help me with the following organic chemistry chapter 7
questions. I keep getting them wrong and I don't know why.
Draw a structural formula for the major organic product of the reaction shown. CH3CH2CH2CH2CH3 + нан HI Draw a structural formula for the major organic product of the reaction shown. CH3 [ CH3 + HCI → Draw a structural formula for the more stable carbocation intermediate formed in the reaction shown. HOD. + HI H3C
Most questions answered within 3 hours.
-
For the reaction 1N2+3H2-----> 2NH3, would the reaction rate
trend be: delta[NH3]/ delta t = -2...
asked 20 minutes ago -
Within your current/past organization, identify a problem/issue
and format a design to address same. You may...
asked 1 minute ago -
A sock stuck to the side of a clothes-dryer barrel has a
centripetal acceleration of 24...
asked 1 hour ago -
A perfect gas undergoes an isentropic process such that its
volume doubles. If the ratio of...
asked 1 hour ago -
list the elements in groups 3A to 6A in the same order as in the
periodic...
asked 1 hour ago -
Estimating effect size. Peng and Chen (2014)
evaluated effect size estimates for various tests. In their...
asked 1 hour ago -
Write a script in MySQL that creates and calls a stored
procedure name test. This procedure...
asked 1 hour ago -
If we test the following: H0: μ = 17
vs. H1: μ ≠ 17 and the...
asked 1 hour ago -
in the past year TVG had revenues of 3 million, cost
of goods sold of $25...
asked 2 hours ago -
4) In a polypeptide, which bond cannot rotate because of its
partial double bond character?
The...
asked 2 hours ago -
Assume that in the short run L = 1,000 and K = 100. 1. What is...
asked 2 hours ago -
At a given temperature, 2.06 atm of H2 and 3.7 atm of Br2 are
mixed and...
asked 2 hours ago