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Draw the structure of each type of compound. a. a d-aldotriose 14.24 c. a four-carbon aldonic...
Classify each monosaccharide in terms of functional group and
number of carbon atoms.
a. HOCH CHC-H OH 0 Ketotetrose 0 Ketopentose 0 O Aldopentose 0 Aldotetrose 0 Ketohexose 0 Ketotriose O Aldotriose O Aldohexose b. HOCH,CHỨCH,OH OH O Ketotetrose O Ketotriose O Ketopentose O Aldotetrose O Ketohexose O Aldopentose O Aldotriose O Aldohexose OOH C. HOCH,CCHCHCHCH,OH ОН ОН 0 Ketopentose Aldotriose Aldotetrose O Aldohexose 0 Ketotriose O Aldopentose o Ketotetrose Ketohexose o OH d. H-CCHCHCH2OH OH O Aldotetrose 0 Ketotetrose...
Draw the structure of each compound
1. Draw the structure of each compound: (a) cis-1,2-Cyclohexanediol (b) Isobutanol (c) 2,4,6-Trinitrophenol (d) (R)-2,2-Dimethyl-3-heptanol (e) Ethylene glycol (0) (s)-2-Methyl-1-butanol 2. Acid-catalyzed hydration of 3,3-dimethyl-1-butene produces 2,3-dimethyl-2-butanol. Show a mechanism for this reaction 3. Acid-catalyzed hydration of 1-methylcyclohexene yields two alcohols. The major product does not undergo oxidation, while the minor product will undergo oxidation. Explain. 4. Using 2-propanol as your only source of carbon, show how you would prepare 2-methyl- 2-pentanol. 5. Identify...
Draw a three dimensional structure for each compound, and star all asymmetric carbon atoms. Draw the mirror image for each structure, and state whether you have drawn a pair of enantiomers or just the same molecule twice. Draw the enantiomers of 1,3-dibromobutane and label them as (R) and (S).
1. Monosaccharide structure Aldohexose: D - talose 1. Draw the aldohexose assigned to you in chain form. 2. How many chiral carbons are there in your hexose? Label all the chiral carbons in your structure above with a asterisk (*). 3. Draw the same aldohexose in its pyranose forms, showing both its a and B anomers. a-anomer: B-anomer: 4. Draw two epimers (one at carbon-3 and another at carbon-4) of your aldohexose in chain form, and give their correct names....
CH,OH b. Is the ketopentose a reducing sugar? c. Is the ketopentose a deoxy sugar? d. Is the ketopentose an amino sugar? e. Draw the L-2-ketopentose that also gives the alcohol sugar above, when treated with H, and Pt. 10.59 a. 10.60 a 10.47 Draw the alcohol sugar, aldonic acid, and uronic acid that can be formed from each monosaccharide. a. D-2-deoxyribose b. L-2-deoxyribose C. the C-3 epimer of D-2-deoxyribose 10.61 10.62 10.48 Draw the alcohol sugar, aldonic acid, and...
Draw the Lewis structure of the compound that forms carbon with silicon. then classify it as ionic or covalent.
Draw dash formula structure of a 5-carbon compound (may be branched or straight chain; and multiple possibilities) with the following functional group: (a) Alkane (b) Alkene (c) Alkyne (d) Alcohol (e) Aldehyde (f) Ketone (g) Ester (h) Nitrile
d) Draw the structure of the most polar compound and draw an arrow (through the structure) representing the overall/net dipole moment of the compound. 3) Suppose that your TLC showed that the compounds had not travelled away from your loading spot. What would be an easy condition to change to make the compounds travel up the TLC plate)? Briefly, state specifically what new condition might you try! (0.5) New conditions you could try is dotting more in the same spot,...
Determine the structure of each compound for each 1H NMR
spectrum. Draw the determined structure and annotate (correlate the
equivalent protons with the corresponding NMR signal(s) in the
spectrum).
Compound C, M = 102.13 g/mol PPM Compound D, M = 136.15 g/mol 12 10 8 6 PPM 4 2 0
Draw the structure of an eight-carbon alkene that would yield
the following compound (and no others) after treatment with ozone
followed by dimethyl sulfide.