Question



2. Assign Ror Sfor each chirality center in the following molecules 3 point OF Is the compound b chiral or achiral? Explain (
0 0
Add a comment Improve this question Transcribed image text
Answer #1

solution: CH3 R- configuration. CH2F R configuration H ot Br R configuration CH2F Horizon at Horizontal line - above the plan③ BD Al I CH3 I HJ LH Brglhu / It u The hydrogen is most reactive when compound reacts with Bradhr because there is formation

Add a comment
Know the answer?
Add Answer to:
2. Assign Ror Sfor each chirality center in the following molecules 3 point OF Is the...
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
  • need help with questions 1-3 1. Assign the absolute configuration (Ror S) of the chiral points...

    need help with questions 1-3 1. Assign the absolute configuration (Ror S) of the chiral points in the molecules below. 2. How many chiral carbons are in the molecule shown below? 3. Draw the molecule below in its chair form and its flipped form. Which one is more stable? Briefly explain why Br

  • 3. R, S Configurations Assign R, S configurations to each indicated chirality center in the molecules...

    3. R, S Configurations Assign R, S configurations to each indicated chirality center in the molecules below. 14. OH 15. COOH ---H CH NH2 HỌN H -CH3 HO alanine norepinephrine - 18. 16. HOC / OHH HV CH; НС . H7 HO COH CH2 dihydrocarvone tartaric acid

  • 4. Assign R or S configuration to each chiral center in each of the following molecules...

    4. Assign R or S configuration to each chiral center in each of the following molecules (A-D). Which are enantiomers and which are diastereoisomer? Hint: redraw the molecules if it makes it easier to visualize or use a modeling kit. H H A В CH Br Hас, Br 'CHs Нo Hас H он Br Br D CHз Hас Н. "CHз но Он CH3

  • 3. Assign the chiral carbons in the following drug molecules as either Ror S. Please write...

    3. Assign the chiral carbons in the following drug molecules as either Ror S. Please write your answers in the boxes provided. HNT NH O levetiracetam antiepileptic metaprolol antihypertensive duloxetine antidepressant HOONEN HO-PLONAN NH, 0 HA tenofovir (Gilead) anti-HIV/AIDS sitagliptin (Merck) oral antihyperglycemic n 4. Draw the structure in line-angle representation for (2R, 4R)-2-chloro-4-ethylheptane:

  • 3. For each of the following chiral molecules, indicate whether the enantiomer shown is the Ror...

    3. For each of the following chiral molecules, indicate whether the enantiomer shown is the Ror Senantiomer. CH3 CH2-CHE чон NH, OH CH=CH2 4. A liquid mixture is comprised of a 50:50 mixture of the following two compounds. Which of the following statements is true? (Choose one) CH3 A) The liquid is a racemate. B) The liquid is a mixture of two constitutional isomers. C) The liquid is a mixture of two unrelated compounds. D) The compounds are identical; it...

  • 1. Chirality (6pts, 2EA) Arethe following carbons indicated by the arrow stereogenic-a chiral carbon center). Write...

    1. Chirality (6pts, 2EA) Arethe following carbons indicated by the arrow stereogenic-a chiral carbon center). Write yes or DATE: 1104.19 No and explain? Н Нс. Br H Hас" Et 2 CONFIGURATIONS (2PTS, IEA) Assign stereoisomer configuration using R or S nomenclature (NOTE: priorities have been preassigned using Cahn-Ingold-Prelog convention) 3. Multiple Choice-Definition (1pt): Define enantiomers: (Circle the correct choice) Molecules with same molecular formula, and connectivity, but differ in 3-dimenisonal space a. b. Molecules with same molecular formula, and connectivity,...

  • 1. Assign R or S configuration to each indicated chirality center (carbon A and B) in...

    1. Assign R or S configuration to each indicated chirality center (carbon A and B) in the following molecule (vitamin C). Which of the following assignments is correct? но OH HO H. a. carbon A (R); carbon B (S) b. carbon A (R); carbon B (R) c. carbon A (S); carbon B (R) d. carbon A (S); carbon B (S) 2. Erythronolide B is the biological precursor of erythromycin, a broad-spectrum antibiotic. How many chirality centers does erythronolide B have?...

  • 2) Which of the following statements is true regarding symmetrical compounds in NMR experiments? 3) How...

    2) Which of the following statements is true regarding symmetrical compounds in NMR experiments? 3) How many H-NMR signals would be in the spectrum for the following compounds? Diasteretopic hyrodgens would produce different signals. 4) What is the splitting pattern for Ha in the following structure? 5) Which of the following statements is true regarding C-NMR? 2. (4 points) Which of the following statements is true regarding symmetrical compounds in NMR experiments? a. a symmetrical compound will always have the...

  • A. Consider the following pairs of structures. Designate each chirality center as (R) or (S) and...

    A. Consider the following pairs of structures. Designate each chirality center as (R) or (S) and identify the relationship between them by describing them as representing enantiomers, diastereomers, constitutional isomers, or two molecules of the same compound. Use handheld molecular models to check your answers. B.  Tartaric acid [HO2CCH(OH)CH(OH)CO2H] was an important compound in the history of stereochemistry. Two naturally occurring forms of tartaric acid are optically inactive. One optically inactive form has a melting point of 210 − 212 °...

  • 1. Predict the products of the following reactions (18 points, 3 each) Catalytic KOH methanol/water solvent...

    1. Predict the products of the following reactions (18 points, 3 each) Catalytic KOH methanol/water solvent Catalytic KOH methanol/water solvent Catalytic KOH methanol water solvent Catalye KOH. 1 equivalent NaOCH.CH ethanol solvent I equivalent NaOCH.CH ethanol solvent 2. Write the product of the following reaction and the full mechanism by which it is formed. Clearly show which steps are reversible and which one step is irreversible. (8 points). 1 equivalent NaOCH CH3 cthanol solvent + excess 3. Circle the most...

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