но OH prortacyelin 8.(10 points)Label each pair of stereoisomers below as: enantiomers b. diastereomers c. identica...
1. (3 points) Label each pair of compounds as enantiomers, diastereomers, constitutional isomers, identical or different. CN Co2H H2NOC CH3 NC H3C H2NOC CO2H ideuhical O HO-/ OH -OH HO- enantiomscs HO.. но OH 3. 1 constituhonal он isomirs 2. (4 points) Use the drawings of TLC plates to answer the Student A c9 Student B
4. Label each pair of stereoisomers below as A,B,C,D a. Enantiomers b. Diastereomers c. Identical d. Meso Compounds a 5 diasteromers e nannamers OH ОН
4. Label each pair of stereoisomers below as A,B,C,D a. Enantiomers b. Diastereomers c. Identical d. Meso Compounds N OH OH 11
Constitutional Isomers-same MF, diff. connectivity Enantiomers-stereoisomers, mirror image, not superimposable Diastereomers-stereoisomers, not mirror image Same-same MF, same connectivity, same spatial arrangement Different-different MF (12 points) 8. In the boxes below, give the relationship between the pairs of molecules. Possible terms are shown at right. Each term may be used more than once and some terms may not be used at all. Cl Br CHy CHs CH and and CHS Cl H Br н CH3 CHs H CHs CHs and CHg...
Pl ease check my work 4. Label each pair of stereoisomers below as A,B,C,D a. Enantiomers b. Diastereomers c. Identical d. Meso Compounds C S А СИ A ОН ОН Я HC -CH₂ 4 се
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...
Carbohydrates 1. Label each of the monosaccharides shown below as a triose, tetrose, pentoso, or hexose. но CH OH HT -он - он Н - ОН но -н но -Н но -н нон сньон он но -н НОН CH OH нон нон нон снон CH OH сон сон H- OH H- -он OH cң, он н-с-он Сн,он снон 2. Label each of the monosaccharides shown above as a ketose or aldose. 3. Identify all of the chiral carbons in the...
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...
What is the relationship between each pair of molecules shown below? H Н3САН нсH3 CH3 identical constitutional isomers enantiomers diastereomers no relationship OH CH3 HO|| І. ОН CH3 CH3 НО! исHз с. тісі
3.30 Are the formulas within each set identical, enantiomers, or diastereomers? and нсін Ay (b) HOH CI . Y нон and Но н y НСІ СІ Н (a) A нон нСІ (c) НО Н НО Н and X Сін 3.31 Which of the following are meso compounds? Br Br b) HCH. НО СН, - Br (а) C HT -C C-c Н H7 он CH Br CH,OH Но ОН 1 CH, (e) / VOH (0) HOH (НОН CH,OH н, CHO ОН...