Why is the answer A? Please explain clearly.
Why is the answer A? Please explain clearly.
Why is the answer A? Please explain clearly.
Why is the answer A? Please explain clearly.
Why is the answer A? Please explain clearly.
Why is the answer A? Please explain clearly.
Why is the answer A? Please explain clearly.
Why is the answer A? Please explain clearly.
Why is the answer A? Please explain clearly.
Why is the answer A? Please explain clearly.
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Why is the answer A? Please explain clearly. Why is the answer A? Please explain clearly....
Prelab Assignment Prior to the laboratory, complete the following Pre-lab Question(s): 1. Cis and Trans isomers of 1,2-dichlorocyclohexane, 1,3-dichlorocyclohexane and 1,4- dichlorocyclohexane - Draw the perspective, Chair and mirror image (if applicable) of each isomer. Perspective (Wedge dash) Chair conformation Drawing Mirror Image chair Chiral? Cis-1,2-dichlorowyclohexane Trans-1.2-dichlorocyclone Is either isomer a mese compound? If yes, draw the plane of symmetry on the mese compound What is the errochemical relationship between these is transiomer? C-1,3-dichlorocyclohexane Trans-1,3-dichloroceae Is either somer amese compound?...
please explain
7. What is the configuration of the following compound? СН3 H-1-ci Cl-- CH2CH3 A) 2S, 3R B) 3R, 3S C) 2S, 3S D) 2R, 3R E) Can't do R and S; the compound is achiral.
c. cis-1-metbylbicylol0.4.4ldecan 24. Which structure is syn? d. trans-1-methylbicyclo[0.4.41derane e. not a.-d с. e. not a.-d 25. Monocyclic alkenes (for example, cyclepropene, cyclobutene, etc.) up to 7 carbons are all? a. b. R C. S d. Z e. not a.-d. 26. The following stereoisomer of a controlled substance is? (Hint: The alcohol is the 1 carbon.) a. 1R, 2R) b. (1R, 25) c. (1S, 2R) d. (1S, 2S) e. not a.-d 27. The carbon with the asterisk is? a. с....
4) Draw the following compounds a. (2S,5R)-5-chloro-2-ethylhexanoic acid b. (1R,2R,4R)-4-ethylcyclohexane-1,2-diol c. (2S,3R)-3-amino-2-phenylbutanal d. (1S,2S,3R)-2-fluoro-3-propylcyclobutanol e. (2E, 7Z)-5-bromo-2,7-nonadiene
Hello, I need help drawing a. to d. Thank you!
lonshid-S(2 9vis 1 Draw the following compounds a. (2S,5R)-5-chloro-2-ethylhexanoic acid b. (1R,2R,4R)-4-ethylcyclohexane-1,2-diol c. (2S,3R)-3-amino-2-phenyl butanal (1S,2S,3R)-2-fluoro-3 -propyl cyclobutanol d. e. (2E, 7Z)-5-bromo-2,7-nonadiene
eneral classification is given to the molecule below? A) primary chloride B) secondary chloride C) tertiary chloride D) vinyl chloride E) benzyl chloride 12. 13) Which of the following is a geminal dihalide? A) cis-1,2-dibromocyclopentane B) 3,3-dichloropentane C) trans-1,4-diiodocyclohexane D) isobutyl chloride E) 1,3-dibromoheptane 13. 15) Which of the following is a secondary alkyl halide? A) methyl bromide B) isopropyl chloride C)-butyl iodide D) propyl bromide E) isobutyl chloride 14. 17) What is the IUPAC name of the compound shown...
Please explain clearly why the answer is correct
Which of these "curved arrows" describe a mechanism for the formation of a carbocation that has roughly the same stability as this one? HHH - H- C- C 70-I CH H H-C-H Н AA only [B] B only [C] C only [D] B and C only [E] A and C only Explanation for your choice (4 pts)
I do not understand why (2) is the correct answer. Please
clearly explain and show .My test is tomorrow. lol Thank you.
The Newman Projection for a portion of the following molecule is given below. H O O Br 7.1. Which of the following describes the H NMR splitting pattern of the methine hydrogen (the one which is detected at the lowest field)? (1) doublet of doublets (2) triplet (3) singlet (4) triplet of quartets
the correct answer is molecule 2. please just explain with A
LOT of detail why please. why is it not 3,4 and 5?
Which of the following molecules will have the second strongest conjugate base? Molecule 1: Molecule 2: Best Avail Molecule 3: Awar Molecule 4: Molecule 5: No att Attad delete closed (a) Molecule 5 (b) Molecule 3 • (c) Molecule 1 x (d) Molecule 4 (e) Molecule 2 x 0% This question is complete and cannot be answered...
Can someone explain why the answer is not
cis-1,2-cyclohexanediol and ethanol?
Question 7 What are the products of the reaction shown below? O CH heat O IH OA. cyclohexanone and ethanol O B. cis-1,2-cyclohexanediol and ethanol O C. trans-1,2-cyclohexanediol and ethanol O D. cyclohexanone and ethanal 0 E. cis-1,2-cyclohexanediol and ethanal