Question
please do all.
7D. Complete the following Fischer projections for all 4 of your models and assign Rand S to all chiral carbons. Label the pa
7A. Complete the following Fischer projections for the three tartaric acid isomers. Label the pair of enantiomers, a pair of
0 0
Add a comment Improve this question Transcribed image text
Answer #1

(0он соби ООО ТЕБЕ НО -н ні — бң и сооч иб-тең — би —СН. И ! сен Соон Сори -cң, СООИ (С) coon (+) (8) на соң We will assign Rcoon — ои cook к Ron coon ho— -н 애 woon (E) IB-H He on coon coon F) olmt@ Both m,n carbon centres are s-configuration Althoug

Add a comment
Know the answer?
Add Answer to:
please do all. 7D. Complete the following Fischer projections for all 4 of your models and...
Your Answer:

Post as a guest

Your Name:

What's your source?

Earn Coins

Coins can be redeemed for fabulous gifts.

Not the answer you're looking for? Ask your own homework help question. Our experts will answer your question WITHIN MINUTES for Free.
Similar Homework Help Questions
  • 5. For the following set of Fischer projections answer each of the questions below by circling...

    5. For the following set of Fischer projections answer each of the questions below by circling the appropriate letter(s) or letter combination(s). Hint: Redraw the Fischer projections with the longest carbon chain in the vertical direction and having similar atoms in the top and bottom portion. Classify all chiral centers in the first structure as R or S absolute configuration. (X pts) a. Which are optically active? b. Which are meso? c. Which is not an isomer with the others?...

  • 19-26 thanks! 19-29* PART 3: 2,3-BUTANEDIOL CH-CH(OH)-CH(OH)-CH, mirror images, not superimposable Build as many models of...

    19-26 thanks! 19-29* PART 3: 2,3-BUTANEDIOL CH-CH(OH)-CH(OH)-CH, mirror images, not superimposable Build as many models of 2,3-butanediol as you can. First, attach two carbons with a single bond. To each carbon add one carbon, one hydrogen, and one oxygen. To complete the structure, Ti the remaining hydrogen atoms. Remember, a model is not different if it is completely superimposable on one already constructed! 13. How many stereochemically different models are possible for 2,3-butanediol? 14. What characteristic does one of these...

  • 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...

  • Name: Matriks No: Quiz 2 22 November 2019 CHM3201 Group 3 Question 1 (4 marks) Assign...

    Name: Matriks No: Quiz 2 22 November 2019 CHM3201 Group 3 Question 1 (4 marks) Assign names for these structures according to IUPAC nomenclature. Assign stereochemistry where necessary. a) Br ÇI Hob) HN+CH2CH2CH3 OH Question 2 (7 marks) a) How many chiral carbons are presence in hexan-3,4-diol? Name: Matriks No: Quiz 2 22 November 2019 CHM3201 Group 3 Question 1 (4 marks) Assign names for these structures according to IUPAC nomenclature. Assign stereochemistry where necessary a) How C4,CH.CH Question 2...

  • 3. Diastereomers and Meso Forms. When a molecule has two or more stereogenic centers, stereoisomers that...

    3. Diastereomers and Meso Forms. When a molecule has two or more stereogenic centers, stereoisomers that are not mirror images can exist; these are called diastereoisomers. Within this general class, there are special types of stereoisomers that are always optically inactive and are called meso forms. Construct a model with four different colored balls about a carbon center. Construct another identical to the first and verify this by the superimposition test. Now remove the same colored balls, blue (C from...

  • are all of these identical? 4. Determine if each of the following structures i) contain chiral centers. Label Chical...

    are all of these identical? 4. Determine if each of the following structures i) contain chiral centers. Label Chical centers with an asterisk. ii) are enantiomers or not. Write "enantiomers" or "identical below each pair. (Hint: determine Ror S for each) a k al identical identical 3 CH | HỌC, OH HOA Hu H + C F ¢ identical ch; HH Br B HC CH, HẠC X 10 identical 3 4 O HC H4 4. 3 . 44 4n/ ТОН...

  • Hello just double checking my ochem study guide, please answer ALL the questions you see below, i...

    Hello just double checking my ochem study guide, please answer ALL the questions you see below, if not let someone else do them please! High rating only given to ALL questions complete Provide the relationship between the two structures shown. In the space provided, indicate S, if the two structures represent the same conformation of the same compound, CF, if the two structures represent different conformations of the same compound, CI, if the two structures are constitutional isomers, E, if...

  • 4. Absolute Configuration and R/S Sequence Rules. In 3 you constructed models with two stereocenters that...

    4. Absolute Configuration and R/S Sequence Rules. In 3 you constructed models with two stereocenters that represented 4 stereoisomers. 2,3-Dibromobutanoic acid exemplifies such a compound, Make models for the isomers of this compound. a. Draw solid/dashed-wedge structures for the 4 possible stereoisomers and label the enantiomers and diastereomers. b. Specify the sequence priority for the substituents on carbon-2 and carbon-3. Label each structure with the proper R/S notation in the drawings above, for example (2R, 35). d. Draw Newman projections...

  • please solve all 4. Enantiomers.- THIS FOLLOWING EXERCISES ON PAGES 6 AND 7 ARE TO BE...

    please solve all 4. Enantiomers.- THIS FOLLOWING EXERCISES ON PAGES 6 AND 7 ARE TO BE DONE AS A GROUP WITH THE LAB INSTRUCTOR!!!! a) Construct a model consisting of a tetrahedral carbon center with four different atoms attached - use white, green, orange and violet balls. Each color represents a different group or atom attached to the central carbon. Does this model have a plane of symmetry? Note 1: a plane of symmetry can be described as a cutting...

  • A. Which of the following Newman projections would represent the least stable conformer of 2,2,3....

    PLEASE HELP WITH ALL. A. Which of the following Newman projections would represent the least stable conformer of 2,2,3.3-tetramethylbutane, looking down the 2,3 bond? H3C H3C H3C H3C CH3 b) CH3 H3C e) a) c) CH3 H3C CH3 CH CH3 CH о он B. which one of the following compounds would be chiral? Br он о он a) но HO O он HO C C. which of the following could potentially be used to distinguish between enantiomers? b) NMR c)...

ADVERTISEMENT
Free Homework Help App
Download From Google Play
Scan Your Homework
to Get Instant Free Answers
Need Online Homework Help?
Ask a Question
Get Answers For Free
Most questions answered within 3 hours.
ADVERTISEMENT
ADVERTISEMENT
ADVERTISEMENT