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2) Put the sun Von the most be conforto 3) Assign Ror S configuration for the...
it would be great if you could explain your answers so that I can understand better...
it would be great if you could explain your answers so that I
can understand better
2) Put the sun Von the most be conforto 3) Assign Ror S configuration for the following compounds: COOH "снусна HANH H OH NO ! CH₂ 3CH3 3 CH₂ COOH 4) Assign the following pairs as enantiomers, diastereomers or meso: CH, CH OH OH Br Br- Br- HB- HH- H -Br Br HH Br IHH MICH, сіну Hн Cats
3. Assign R or S configuration to the following molecules: Br F Н. F H- Br...
3. Assign R or S configuration to the following molecules: Br F Н. F H- Br CH, Br CHECH, H CH2CH3 CH2CH3 CH, CH, -CHE OH H CH=CH2 H3CH2 HY CH(CH3)2 CH 4. Label each pair of stereoisomers below as A,B,C,D a Enantiomers b. Diastereomers Identical d Meso Compounds
3. Assign Rors configuration to the following molecules: - Br Br F Br -CH CH.CH H...
3. Assign Rors configuration to the following molecules: - Br Br F Br -CH CH.CH H CH2CHE CH2CH CH, CH -CH, OH H -CH=CH2 H3C 7 Сн, HI CH(CH3)2 4. Label each pair of stereoisomers below as A,B,C,D a. Enantiomers b. Diastereomers c. Identical d. Meso Compounds u 5. Write the complete stepwise mechanism for this reaction. Show all electron flow with arrows and show all intermediate structures. (10 Points) BE CHO -Br (or CI) Br
3. Assign Ror S configuration to the following molecules: Br 1 F H- F H F...
3. Assign Ror S configuration to the following molecules: Br 1 F H- F H F Br Br -CHO CH=CH2 S R R H CH2CH3 CH2CH3 --CH₃ CH3 CH2 H -CH=CH2 CH3 H3C HY -CH(CH3)2 OH
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...
3. Assign R or S configuration to the chirality centers of the following molecules. ҫн, сн,...
3. Assign R or S configuration to the chirality centers of the following molecules. ҫн, сн, b) но н H Br COOH c) H CH COOH CH,CH н. сн,Cн он HO d) H Br H Br h) CH CH,о, g) HO Н СООН CH hway.com
Please answer all three if possible but mainly number 5 Br SCHLECH, 3. Assign R or...
Please answer all three if possible but mainly number 5
Br SCHLECH, 3. Assign R or Sconfiguration to the following molecules: Br F H. I H Br CH F F I . CH2CH3 CH2CH3 CH3CH -CH3 OH CH=CH2 H3C Сн, H "CH(CH3)2 4. Label each pair of stereoisomers below as A,B,C,D a Enantiomers b. Diastereomers c. identical d. Meso Compounds GH 5. Write the complete stepwise mechanism for this reaction. Show all electron flow with arrows and show all intermediate...
1.) Name the following compounds including stereochemistry. + Br 2.) Assign configurations to each of the...
1.) Name the following compounds including stereochemistry. + Br 2.) Assign configurations to each of the chiral centers and circle the stereochemical relationship of the two compounds shown below in Fischer notation? CH3 C2H5 Br- H CH HCI Brt CzH5 A) enantiomers. B) diastereomers - C) constitutional isomers- D) cis/trans - isomers E) meso - same structure CH3 3.) Draw the structure of the meso form of 1,3-dichlorocyclopentane. Take particular care to indicate three-dimensional stereochemical detail properly. -
7. Refer to Exhibit 5-3. The configuration of this carbon atom (E) 15 Exhibit 5-4 Consider...
7. Refer to Exhibit 5-3. The configuration of this carbon atom (E) 15 Exhibit 5-4 Consider the structure of streptimidone to answer the following question(s): OH OH нс н stopuklone ĄCH 8. Refer to Exhibit 5-4. Assign Ror Sconfiguration to each chirality center indicated in streptimidone. 9. Refer to Exhibit 5-4. Will streptimidone have a meso stereoisomer? Explain your answer. Exhibit 5-5 Label each pair of stereoisomers below as: a. enantiomers b. diastereomers c. identical Place the letter of the...
2. Mark all stereocenters with an asterisk (*) and assign the configuration (R or S) for...
2. Mark all stereocenters with an asterisk (*) and assign the configuration (R or S) for each. Also write whether the molecule is chiral, achiral, or meso (3 pts each) H CH2OH b. c. tch Br Сн, 3. Name the following compounds (2 pts each) Br b.
it would be great if you could explain your answers so that I
can understand better
2) Put the sun Von the most be conforto 3) Assign Ror S configuration for the following compounds: COOH "снусна HANH H OH NO ! CH₂ 3CH3 3 CH₂ COOH 4) Assign the following pairs as enantiomers, diastereomers or meso: CH, CH OH OH Br Br- Br- HB- HH- H -Br Br HH Br IHH MICH, сіну Hн Cats
3. Assign R or S configuration to the following molecules: Br F Н. F H- Br CH, Br CHECH, H CH2CH3 CH2CH3 CH, CH, -CHE OH H CH=CH2 H3CH2 HY CH(CH3)2 CH 4. Label each pair of stereoisomers below as A,B,C,D a Enantiomers b. Diastereomers Identical d Meso Compounds
3. Assign Rors configuration to the following molecules: - Br Br F Br -CH CH.CH H CH2CHE CH2CH CH, CH -CH, OH H -CH=CH2 H3C 7 Сн, HI CH(CH3)2 4. Label each pair of stereoisomers below as A,B,C,D a. Enantiomers b. Diastereomers c. Identical d. Meso Compounds u 5. Write the complete stepwise mechanism for this reaction. Show all electron flow with arrows and show all intermediate structures. (10 Points) BE CHO -Br (or CI) Br
3. Assign Ror S configuration to the following molecules: Br 1 F H- F H F Br Br -CHO CH=CH2 S R R H CH2CH3 CH2CH3 --CH₃ CH3 CH2 H -CH=CH2 CH3 H3C HY -CH(CH3)2 OH
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...
3. Assign R or S configuration to the chirality centers of the following molecules. ҫн, сн, b) но н H Br COOH c) H CH COOH CH,CH н. сн,Cн он HO d) H Br H Br h) CH CH,о, g) HO Н СООН CH hway.com
Please answer all three if possible but mainly number 5
Br SCHLECH, 3. Assign R or Sconfiguration to the following molecules: Br F H. I H Br CH F F I . CH2CH3 CH2CH3 CH3CH -CH3 OH CH=CH2 H3C Сн, H "CH(CH3)2 4. Label each pair of stereoisomers below as A,B,C,D a Enantiomers b. Diastereomers c. identical d. Meso Compounds GH 5. Write the complete stepwise mechanism for this reaction. Show all electron flow with arrows and show all intermediate...
1.) Name the following compounds including stereochemistry. + Br 2.) Assign configurations to each of the chiral centers and circle the stereochemical relationship of the two compounds shown below in Fischer notation? CH3 C2H5 Br- H CH HCI Brt CzH5 A) enantiomers. B) diastereomers - C) constitutional isomers- D) cis/trans - isomers E) meso - same structure CH3 3.) Draw the structure of the meso form of 1,3-dichlorocyclopentane. Take particular care to indicate three-dimensional stereochemical detail properly. -
7. Refer to Exhibit 5-3. The configuration of this carbon atom (E) 15 Exhibit 5-4 Consider the structure of streptimidone to answer the following question(s): OH OH нс н stopuklone ĄCH 8. Refer to Exhibit 5-4. Assign Ror Sconfiguration to each chirality center indicated in streptimidone. 9. Refer to Exhibit 5-4. Will streptimidone have a meso stereoisomer? Explain your answer. Exhibit 5-5 Label each pair of stereoisomers below as: a. enantiomers b. diastereomers c. identical Place the letter of the...
2. Mark all stereocenters with an asterisk (*) and assign the configuration (R or S) for each. Also write whether the molecule is chiral, achiral, or meso (3 pts each) H CH2OH b. c. tch Br Сн, 3. Name the following compounds (2 pts each) Br b.
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