Homework Answers
1=R
2=S
3=S
4=S
5=R
6=S
7=R
8=R
9=S
10=No chiral
11=No chiral
12=S
13=R
14=S
15=S
16=R
17=S
18=S
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Organic Chemistry I Test 2 Extra Stereochemistry Practice Problems Page 1: Designate R/S Page 2:...
designate the R/S configuration for any chiral centers нсн, но, сня H.CH, H, CH3 Но, |...
designate the R/S configuration for any chiral centers
нсн, но, сня H.CH, H, CH3 Но, | | H NH20 Кн 23, HC NHA 24. нсн, нсна H CH3 нон Дн 26 но сн, .. .CH OH нд но со Р o . 28 ноги нас < HO 29. Но LOH не 30.
designate R/S configuration R-configuration configuration 15. ö lö H, OH CHE 18. 17. HECO HO Rco...
designate R/S configuration
R-configuration configuration 15. ö lö H, OH CHE 18. 17. HECO HO Rco Nh-c Answer key correct but Error in movie for 16. s -cousuvachu H OH H CHI нон HEN2 19. I NH, NH2 Br., CHE 21. H 20, он Answer key correct but Error in movie for 20. нох | H NHÔ нсн. н. сня Η HO...IH 23. H₃C NH₂ H, CH, HO, CHE H, CH3 H., CHE нсна АН 26. HO CHE Hнсн,он HOYO...
A. Designate the R/S configuration for any chiral centers in the following molecules. Brn HN нон онон NH - Чон 2 он...
A. Designate the R/S configuration for any chiral centers in the following molecules. Brn HN нон онон NH - Чон 2 оноо H.CH HOOH нсн соо HOH нон „о ако ен, и Answer key correct but Error in movie for 16. нон нан, Br. CH нхл OH Answer key comect but Em for 21. н NH но сн, нан, қсн, но, 22 но не 24 No 2 нын, нсн, нан, ess Хүн c. 26. но сни нога но он но...
Handout Stereochemistry 1. Designate each of the chirality centers as R or S. Then identify the...
Handout Stereochemistry 1. Designate each of the chirality centers as R or S. Then identify the relationship between the two molecules as enantiomers, diastereomers, identical, or non-related. Bс нс си, сн, H Br H (e) (a) and and сн н" Вr нс н н Br ис, и нс, H and and Br (b) СH Bе Br HT Br н H Br. Br H CH, Br () Нс and and но Br CH Br НаС. H, Br. CH H- (b) (d)...
H 9. For each molecule: 1) Identify all possible enantiomers and distinguish those that are enantiomers, diastereomers...
H 9. For each molecule: 1) Identify all possible enantiomers and distinguish those that are enantiomers, diastereomers and meso compounds. II) Assign the absolute configuration of chiral carbons in each molecule OCH3 HO+Br HS+CN H2N-CH3 HOSH Он HO+CH3 н OCH3 Сн, ососна Br +D HOCH HC-BrHN+Br CH 8. For the following compounds, assign the absolute configuration for those with chiral carbons and identify those that are NOT enantiomers HO C-C-OHY -CCIN 13CH3 HAN CH3 CH3 осі H-CH3 H2N+CH H O+COOH...
Organic Chemistry please help asap 70. What nucleophiles wou cleophiles would form the following compounds as...
Organic Chemistry please help asap
70. What nucleophiles wou cleophiles would form the following compounds as a result of reacting with l-iodobutane? OH SH 11. Draw (R)-2-bromopentane + CHO b. (R)-3-bromo-3-methylheptane + CH,OH c. benzyl chloride + CH CH OH te tollowing reactions: if the products can exist as stereoisomers, show what striscmers are obtained d. allyl chloride + CHOH e. 1-bromo-2-butene + CHO 1. l-bromo-2-butene + CH OH the products obtained from the solvolysis of each of the following...
having trouble with R and S configuration, can someone help out with this sheet? 17 Br>Cl'7...
having trouble with R and S configuration, can someone help out
with this sheet?
17 Br>Cl'7 S"7 F>ONTO77i77 H 1. Determine the configuration (R or S) of each of the following molecules: (Ph phenyl, a benzene ring as a group) CH-CH3 b. CHs с. но NH2 d. он COOH Ph H Hас CH2CH3 H2N CH&CH NH2 NH2 f. Ph CH3 Ph CHs h. H i. OH c lCOOH н.сн,с F Н.с NH2 h. COOH CHs CH2CH H2N 2. Label the...
Need help with the R and S configurations for the two chair questions numbered 1 and...
Need help with the R and S configurations for the two chair
questions numbered 1 and 2 in pink.
Assign each of the indicated asymmetric carbons as either (R) or (S). OCH CN СНО СH-ОН н н. OH Н н Br CH3 CH3 СООН С(CH)3 CH=CH2 Br OH CI н- но- H C(CH3)3 CH3 CF2CH3 енз
1. For each of the following reactions, write S if it is a substitution and E...
1. For each of the following reactions, write S if it is a substitution and E if it is an elimination. Also write R for all of those that are also rearrangements. CH-Oн heat NaOCHs + HBr HG OH Nal Hо acetone NaBr +HBr 2. Predict which reactions proceeded by an SN1, SN2, El or E2 mechanism: NaOCH CH +NaBr оснCH Носн,сн, 50° +NaCl Nal DMSO, 45 Br NaOCHa +NaBr +HOCH Носн, 100° но +HI acetone, 50 HSO +HO HO,...
please help with this page! CHEM211-Summer 2019 Stereochemistry Part 2) Homework 4 1) What type of...
please help with this page!
CHEM211-Summer 2019 Stereochemistry Part 2) Homework 4 1) What type of isomers are CH3CH2OCH3 and CH3CH CH2OH? constitutional B) symmetrical conformational C) configurational E) stereochemical CH сн What is the relationship between the following compounds? 2) HCCI and H CHCI CH constitutional isomers diastercomers superimposable without bond rotation B) enantiomers D) conformational isomers A) C) E) 3) What is the relationship between the structures shown below? diastercoma constitutional isomers conformational isomers sonfigurational isomers enantiomers A)...
designate the R/S configuration for any chiral centers
нсн, но, сня H.CH, H, CH3 Но, | | H NH20 Кн 23, HC NHA 24. нсн, нсна H CH3 нон Дн 26 но сн, .. .CH OH нд но со Р o . 28 ноги нас < HO 29. Но LOH не 30.
designate R/S configuration
R-configuration configuration 15. ö lö H, OH CHE 18. 17. HECO HO Rco Nh-c Answer key correct but Error in movie for 16. s -cousuvachu H OH H CHI нон HEN2 19. I NH, NH2 Br., CHE 21. H 20, он Answer key correct but Error in movie for 20. нох | H NHÔ нсн. н. сня Η HO...IH 23. H₃C NH₂ H, CH, HO, CHE H, CH3 H., CHE нсна АН 26. HO CHE Hнсн,он HOYO...
A. Designate the R/S configuration for any chiral centers in the following molecules. Brn HN нон онон NH - Чон 2 оноо H.CH HOOH нсн соо HOH нон „о ако ен, и Answer key correct but Error in movie for 16. нон нан, Br. CH нхл OH Answer key comect but Em for 21. н NH но сн, нан, қсн, но, 22 но не 24 No 2 нын, нсн, нан, ess Хүн c. 26. но сни нога но он но...
Handout Stereochemistry 1. Designate each of the chirality centers as R or S. Then identify the relationship between the two molecules as enantiomers, diastereomers, identical, or non-related. Bс нс си, сн, H Br H (e) (a) and and сн н" Вr нс н н Br ис, и нс, H and and Br (b) СH Bе Br HT Br н H Br. Br H CH, Br () Нс and and но Br CH Br НаС. H, Br. CH H- (b) (d)...
H 9. For each molecule: 1) Identify all possible enantiomers and distinguish those that are enantiomers, diastereomers and meso compounds. II) Assign the absolute configuration of chiral carbons in each molecule OCH3 HO+Br HS+CN H2N-CH3 HOSH Он HO+CH3 н OCH3 Сн, ососна Br +D HOCH HC-BrHN+Br CH 8. For the following compounds, assign the absolute configuration for those with chiral carbons and identify those that are NOT enantiomers HO C-C-OHY -CCIN 13CH3 HAN CH3 CH3 осі H-CH3 H2N+CH H O+COOH...
Organic Chemistry please help asap
70. What nucleophiles wou cleophiles would form the following compounds as a result of reacting with l-iodobutane? OH SH 11. Draw (R)-2-bromopentane + CHO b. (R)-3-bromo-3-methylheptane + CH,OH c. benzyl chloride + CH CH OH te tollowing reactions: if the products can exist as stereoisomers, show what striscmers are obtained d. allyl chloride + CHOH e. 1-bromo-2-butene + CHO 1. l-bromo-2-butene + CH OH the products obtained from the solvolysis of each of the following...
having trouble with R and S configuration, can someone help out
with this sheet?
17 Br>Cl'7 S"7 F>ONTO77i77 H 1. Determine the configuration (R or S) of each of the following molecules: (Ph phenyl, a benzene ring as a group) CH-CH3 b. CHs с. но NH2 d. он COOH Ph H Hас CH2CH3 H2N CH&CH NH2 NH2 f. Ph CH3 Ph CHs h. H i. OH c lCOOH н.сн,с F Н.с NH2 h. COOH CHs CH2CH H2N 2. Label the...
Need help with the R and S configurations for the two chair
questions numbered 1 and 2 in pink.
Assign each of the indicated asymmetric carbons as either (R) or (S). OCH CN СНО СH-ОН н н. OH Н н Br CH3 CH3 СООН С(CH)3 CH=CH2 Br OH CI н- но- H C(CH3)3 CH3 CF2CH3 енз
1. For each of the following reactions, write S if it is a substitution and E if it is an elimination. Also write R for all of those that are also rearrangements. CH-Oн heat NaOCHs + HBr HG OH Nal Hо acetone NaBr +HBr 2. Predict which reactions proceeded by an SN1, SN2, El or E2 mechanism: NaOCH CH +NaBr оснCH Носн,сн, 50° +NaCl Nal DMSO, 45 Br NaOCHa +NaBr +HOCH Носн, 100° но +HI acetone, 50 HSO +HO HO,...
please help with this page!
CHEM211-Summer 2019 Stereochemistry Part 2) Homework 4 1) What type of isomers are CH3CH2OCH3 and CH3CH CH2OH? constitutional B) symmetrical conformational C) configurational E) stereochemical CH сн What is the relationship between the following compounds? 2) HCCI and H CHCI CH constitutional isomers diastercomers superimposable without bond rotation B) enantiomers D) conformational isomers A) C) E) 3) What is the relationship between the structures shown below? diastercoma constitutional isomers conformational isomers sonfigurational isomers enantiomers A)...
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