I just want to confirm that I did this correctly. I am drawing 2 products from the first present reagent. If it first combines with H-Br, then H-Cl. Are my products correct and is it correct that this is not a racemic mixture?
Also I forget to add the Br in the first product. Also is the first product racemic??
Homework Answers
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I just want to confirm that I did this correctly. I am
drawing 2 products from...
Did I do this problem correctly? I was asked to show products and asked for each...
Did I do this problem correctly? I was asked to show
products and asked for each product formed after a step if it's
racemic or not? Please correct anything that seems wrong.
Bllz CH-CH₂ H₂ C - Is this Racem? (Y/N) (I think CH₂ proche of H2O NaOH final racomic Tautomerization tracom -CH-CH3 H₂ C- CH - CH3 OC!
I am not sure what I did wrong. I believe the answer to the first portion...
I am not sure what I did wrong. I believe the answer to the
first portion is correct, but I am not sure how to approach the
second. Please be very clear in drawing the mechanism and final
product. Please clearly circle the answers.
D CHANH dana -CH2NH-CCH2- o H2O H2SO4 Hoo a. Draw the structure of the tetrahedral intermediate INITIALLY-FORMED in the reaction shown • You do not have to consider stereochemistry. • Do not include counter-ions, e.g., Na",...
Did I identify these reactions correctly and did I draw the correct products? conclusion you did....
Did I identify these reactions correctly and did I
draw the correct products?
conclusion you did. Then show and label the appropriate "product(s) with the correct stereochemistry where applicable!!! Det OH-tertiary alcohol (1) pe H.SO (H30 t) = Werk batet) A Heat present 111CH (mayor product Istrong medieophile) CH,CHS No meat Sn2 CH ₂ CH as CitschacHaciz IS CH 2. Strom bate-> NaNH Pakyl natide O con Strong quclesi(12) o Na acetone aproic SolventLSN) a L.6(E) Strong CHOD )-752 CH...
I'm not sure if 4 is correct so I just wanted some clarification, and for 5...
I'm not sure if 4 is correct so I just wanted some
clarification, and for 5 I also am not sure as I need more
reasoning for why product B was formed!
4. Propose an arrow-pushing mechanism for the reaction below. 1. Cl₂, H₂O 2. NaH HO O-H Loh HOH Na-u 00 27, 5. During a “routine" bromination of an alkene, a team of researchers at the University of Georgia were surprised to find that got a significant amount of...
Just need to check if I am doing this correctly, I want to make sure my...
Just need to check if I am doing this correctly, I want to make
sure my answers are correct for the parts I have answered... also I
am confused how to answer question C. Thanks!!!!
2. Tom and Lindsey have just given birth to their fourth child, a girl named Katie. Soon after Katie's birth, Tom and Lindsey leamed that a routine newborn screening test showed that Katie has phenylketonuria (PKU), a genetic disorder in which phenylalanine cannot be digested...
hi, did I do the second data correctly? also can someone help me with the third...
hi, did I do the second data correctly? also can someone help
me with the third data how to do it
II, DATA and RESULTS: A INITIAL SOLUTIONS: In the space provided, fill in the information for each of the initial aqueous solutions. Solution # ution Formu Ammonium Carbonate NH4 CO Clear Barium Acetate(C CH COO Ba Calcium Chloride CaCl2 Ca Cl Clear Copper BromideCu(Br) Cu Br Bluish B) OBSERVATIONSDWrite general observations for each reaction, and state if precipitate (PPT)...
I have completed some answers! I just really really need help with the rest! I am...
I have completed some answers! I just really really need help
with the rest! I am so lost! please help me, if you can!
What information do you need? Can you see the pictures that I
posted?
#2-6 are using the FIGURE from question #2
#7-8 go together and uses #7 FIGURE
#9-12 uses #9"s FIGURE but #11 and #12 compares the two FIGURES
from #7	
#13 and 14 are together
# 15 and # 16 are their own problems...
I need help with questions 5, 6, & 7. The FTIR and NMR is provided. I...
I need help with questions 5,
6, & 7. The FTIR and NMR is provided. I also need help creating
a reaction mechanism using the following:
Starting material: methyl acetate.
Solvent: diethyl ether
Reagent: sodium methoxide
Product: methyl acetoacetate
THANK YOU!!!!!
11-8: Claisen Condensation - 1 For this assignment, the target compound that you should synthesize is methyl acetoacetate.This is another carbonyl addition variation. Examine the product and determine which ester is the nucleophile and which is the electrophile. Keep...
I need help with questions 5, 6, & 7. The FTIR and NMR is provided. I...
I need help with questions 5, 6, & 7. The FTIR and NMR is
provided. I also need help creating a reaction mechanism using the
following:
Starting material: 1,7-Dimethyl-heptanedioate
Solvent: Diethyl ether
Reagent: sodium methoxide
Product: 3-oxo-cyclohexane carboxylic acid methyl ester
THANK YOU!!!!!
Ö 11-11: Dieckmann Reaction For this assignment, the target compound that you should synthesize is 2-oxo-cyclohexane carboxylic acid methyl ester.This is an intramolecular carbonyl addition variation. Examine the product and determine which ester is the nucleophile and...
CHEM 2343A HOMEWORK W13 Name: DUE 11/18/19 at 9:10 AM There are total of 4 questions...
CHEM 2343A HOMEWORK W13 Name: DUE 11/18/19 at 9:10 AM There are total of 4 questions on this homework assignment 1. For the reaction outlined below in la and I draw out the reaction mechanism using arrow formalism to describe how the reaction below occurs. Be sure to draw out all action intermediates & the moment of all electrons needed to justify the formation of the indicand product. You do not need to add in any reagents that are not...
Did I do this problem correctly? I was asked to show
products and asked for each product formed after a step if it's
racemic or not? Please correct anything that seems wrong.
Bllz CH-CH₂ H₂ C - Is this Racem? (Y/N) (I think CH₂ proche of H2O NaOH final racomic Tautomerization tracom -CH-CH3 H₂ C- CH - CH3 OC!
I am not sure what I did wrong. I believe the answer to the
first portion is correct, but I am not sure how to approach the
second. Please be very clear in drawing the mechanism and final
product. Please clearly circle the answers.
D CHANH dana -CH2NH-CCH2- o H2O H2SO4 Hoo a. Draw the structure of the tetrahedral intermediate INITIALLY-FORMED in the reaction shown • You do not have to consider stereochemistry. • Do not include counter-ions, e.g., Na",...
Did I identify these reactions correctly and did I
draw the correct products?
conclusion you did. Then show and label the appropriate "product(s) with the correct stereochemistry where applicable!!! Det OH-tertiary alcohol (1) pe H.SO (H30 t) = Werk batet) A Heat present 111CH (mayor product Istrong medieophile) CH,CHS No meat Sn2 CH ₂ CH as CitschacHaciz IS CH 2. Strom bate-> NaNH Pakyl natide O con Strong quclesi(12) o Na acetone aproic SolventLSN) a L.6(E) Strong CHOD )-752 CH...
I'm not sure if 4 is correct so I just wanted some
clarification, and for 5 I also am not sure as I need more
reasoning for why product B was formed!
4. Propose an arrow-pushing mechanism for the reaction below. 1. Cl₂, H₂O 2. NaH HO O-H Loh HOH Na-u 00 27, 5. During a “routine" bromination of an alkene, a team of researchers at the University of Georgia were surprised to find that got a significant amount of...
Just need to check if I am doing this correctly, I want to make
sure my answers are correct for the parts I have answered... also I
am confused how to answer question C. Thanks!!!!
2. Tom and Lindsey have just given birth to their fourth child, a girl named Katie. Soon after Katie's birth, Tom and Lindsey leamed that a routine newborn screening test showed that Katie has phenylketonuria (PKU), a genetic disorder in which phenylalanine cannot be digested...
hi, did I do the second data correctly? also can someone help
me with the third data how to do it
II, DATA and RESULTS: A INITIAL SOLUTIONS: In the space provided, fill in the information for each of the initial aqueous solutions. Solution # ution Formu Ammonium Carbonate NH4 CO Clear Barium Acetate(C CH COO Ba Calcium Chloride CaCl2 Ca Cl Clear Copper BromideCu(Br) Cu Br Bluish B) OBSERVATIONSDWrite general observations for each reaction, and state if precipitate (PPT)...
I have completed some answers! I just really really need help
with the rest! I am so lost! please help me, if you can!
What information do you need? Can you see the pictures that I
posted?
#2-6 are using the FIGURE from question #2
#7-8 go together and uses #7 FIGURE
#9-12 uses #9"s FIGURE but #11 and #12 compares the two FIGURES
from #7	
#13 and 14 are together
# 15 and # 16 are their own problems...
I need help with questions 5,
6, & 7. The FTIR and NMR is provided. I also need help creating
a reaction mechanism using the following:
Starting material: methyl acetate.
Solvent: diethyl ether
Reagent: sodium methoxide
Product: methyl acetoacetate
THANK YOU!!!!!
11-8: Claisen Condensation - 1 For this assignment, the target compound that you should synthesize is methyl acetoacetate.This is another carbonyl addition variation. Examine the product and determine which ester is the nucleophile and which is the electrophile. Keep...
I need help with questions 5, 6, & 7. The FTIR and NMR is
provided. I also need help creating a reaction mechanism using the
following:
Starting material: 1,7-Dimethyl-heptanedioate
Solvent: Diethyl ether
Reagent: sodium methoxide
Product: 3-oxo-cyclohexane carboxylic acid methyl ester
THANK YOU!!!!!
Ö 11-11: Dieckmann Reaction For this assignment, the target compound that you should synthesize is 2-oxo-cyclohexane carboxylic acid methyl ester.This is an intramolecular carbonyl addition variation. Examine the product and determine which ester is the nucleophile and...
CHEM 2343A HOMEWORK W13 Name: DUE 11/18/19 at 9:10 AM There are total of 4 questions on this homework assignment 1. For the reaction outlined below in la and I draw out the reaction mechanism using arrow formalism to describe how the reaction below occurs. Be sure to draw out all action intermediates & the moment of all electrons needed to justify the formation of the indicand product. You do not need to add in any reagents that are not...
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