Q: For 2-bromo-3-chlorobutane: a. Draw the 2-D Lewis structure b. How many stereoisomers are possible…
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Q: Convert each compound to a Fischer projection formula. Сно но b. a. HO. HOCH, CHO HOCH,
A: a) The Fischer projection of the given compound is,
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A: (a)
Q: 士 0. 1. 8. Identify (circle) all the chirality centers in the oral contraceptive, Mestranol.
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Q: Convert the Fischer projection to a perspective formula.
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Q: (a) Butan-2-ol (b) 1,2-dibromobutane (c) (d) CH,OH он HOH,C -CHO H3C OH
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Q: Write "most" under the member of each trio which is most stable. Write "least" under the member of…
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Q: The following compound has how many stereogenic centers? CH3
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Q: Convert the Fischer projection to a perspective formula.
A: To convert the Fischer projection into perspective formula , firstly R and S confirmation is…
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Q: (е) CНзCH(NH2)CH(NH2)CHз (f) CH;CH(OH)CH(OH)CH2OH (g) (h) CH3CH2CH(CI)CH(CI)CH2CH3 OH OH…
A: depending on the three dimensional orientation of the molecule there can be some stereo isomer .
Q: III. Consider the compound below. H. F OH HO HO- (Atomic number: H-1, C-6, O-8, F-9) a. How many…
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Q: Convert the Fischer projection to a perspective formula. H-COO-CH2CH3-CH3
A: To convert from Fischer to perspective formula
Q: Convert each compound to a Fischer projection formula.
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Q: Draw Fischer projections for the four stereoisomers of 2-bromo-3-chlorobutane, label them (2R,3R),…
A: We have find out the four stereoisomers of 2-bromo-3-chlorobutane.
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A:
Q: Draw each compound in its most symmetric conformation, star (*) any asymmetric carbon atoms, and…
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Q: 17. Draw the Fischer projection of the following compound. OH MeO2C. CO,Me ОН 18. Name this compound…
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Q: Locate the stereogenic center in each compound and draw both enantiomers.
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Q: '. How many chirality center/s are in the molecule shown below? Show them Br H;C-CH,CH(CH3)CHCH3
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Q: Consider (2R,3R)-2,3-dioidobutane: (a)Draw a Fischer Projection of this structure with C1 on top…
A: The structure of 2,3-diiodobutane is as follows:
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Q: a a) Convert the following perspective drawing to a Fischer projection: と-o+ HO
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A: Haworth structure of Glucose is represented as follows. Correct option is D.
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Q: Re-draw each Fischer projection formula using wedges and dashed wedgesfor the stereogenic center,…
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Q: 10. Draw all stereoisomers of CH3CHCI-CHBRCH3 as Fischer projections and label the R, S…
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- Consider (2R,3R)-2,3-dioidobutane: (a)Draw a Fischer Projection of this structure with C1 on top and C4 on bottom. (b)Draw a Newman Projection of of the meso compound of 2,3-dibromobutane looking down the C2-C3 bondwith C2 in front, and label your asymmetric carbons as S or R.Please do parts A and B Consider (2R,3R)-2,3-diidobutane: (a) Draw a Fischer Projection of this structure with C1 on top and C4 on bottom. (b) Draw a Newman Projection of of the meso compound of 2,3-dibromobutane looking down the C2-C3 bond with C2 in front, and label your asymmetric carbons as S or R.Draw out the most and least preferred chair conformation of the compound below. Draw their boat conformation, and then their 2nd chair conformation. How manystereoisomers do the compound have?
- Part D. Do the two structures A and B of each pair drawn below represent the same molecule, constitutional isomers, or stereoisomers? If A and B are stereoisomers, further classify them as enantiomers or diastereomers.Draw Newman Projections representing the two highest and two lowest energy conformers of (3S,4S)-4-tert-butyl-2,3-dimethyloctane as viewed along the C3-C4 bond. b.) Label each conformer with theappropriate description then analyze them and rank their energies and explain your reasoning by specifyingthe types of interactions. (Hint: Draw the first and then rotate only the front or back carbon)Please answer this NEATLY, COMPLETELY, and CORRECTLY for an UPVOTE. a. Do enantiomers have the same molecular formula? b. Does one structural formula represent both members of a pair of enantiomers? c. Are enantiomers stereoisomers?
- Given the following structure and numbering: (a) Label the stereocenters of A as R or S and draw a Fischer Projection of the enantiomer of A with C1on top and C4 on bottom. (b) Draw a Newman Projection of a diastereomer of A looking down the C2-C3 bond with C2 in front.Draw all possible stereoisomers for the molecule in Fischer projection and label the srelationship between each of the isomer.A trisubstituted cyclohexane compound is given below in its chair conformation. Draw the corresponding planar (overhead) representation, using wedge-and-dash bonds to indicate the substituent positions. Include the hydrogen atoms on the chirality centers (asymmetric carbons). Be sure that both wedge/dash bonds are drawn on the outside of the ring, or else the stereochemistry may be interpreted as square planar.
- Why is molecule b more stable than a in chair conformation?label the stereocenters r,s,e,z and specify if any are meso. whats are the products to each orher? draw the chair conformationd and explain which one is the most stable for both products. are ha and hb homo/enantio/diasterio/hetero topic? also hc and hd.Draw (1R,3S)-1,3-dimethylcyclohexane, in its minimum energy conformation. Then draw the Newman Projection for this structure with the correct stereochemistry and in its minimum energy state.