Draw the skeletal ("line") structure of an aldehyde with 3 carbons in the main chain and 1 methyl group substituent. Click and drag to start drawing a structure. X :0
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- Define the following terms: a. reducing sugar b. alditol c. enediol d. acetal e. ketalDraw one aromatic polar amino acid at pH 7. Label with full name, three letter abbreviation, and single letter symbol.draw the following amino acid chains and give the single and three letter abbreviations for cysteine
- How would a monosaccharide with 7 C atoms & a ketone group be classified? Choose your answer from the following options. EXPLAIN. Aldoheptose Ketoheptose Heptoaldose Heptoketose Aldose heptose Ketose heptoseIdentify ALL the CORRECT statements regarding the compound shown below. SELECT ALL THAT APPLY A. The compound is a heterocycle B. The compound is found in DNA C. The compound is a pentose sugar D. The compound is a purineComplete the following table by providing the Fischer and Haworth Projections of the given sugars. In the Fischer Projection put an asterisk (*) mark in the chiral centers of the molecule. Sugar Fischer Projection Haworth Projection (Complete) alpha-anomer Haworth Projection (Abbreviated) beta-anomer D-Mannose D-Xylose L-Lyxose
- Complete the following table by providing the Fischer and Haworth Projections of the given sugars. In the Fischer Projection put an asterisk (*) mark in the chiral centers of the molecule. Sugar Fischer Projection Haworth Projection (Complete) alpha-anomer Haworth Projection (Abbreviated) beta-anomer L-Galactose L-Fructose D- XyloseWhich of the following is a fatty acid with this notation, 16:0 Stearic acid Myristic acid Lauric acid Palmitic acidFind the isoelectric point by typing Gly-Asp-Ala tripeptide.
- The synthetic process by which monomers are covalently linked is (a) hydrolysis (b) isomerization (c) condensation (d) glycosidic linkage (e) ester linkageComplete the following table by providing the Fischer and Haworth Projections of the given sugars. In the Fischer Projection put an asterisk (*) mark in the chiral centers of the molecule. Sugar Fischer Projection Haworth Projection (Complete) alpha-anomer Haworth Projection (Abbreviated) beta-anomer L-Galactose L-Fructose D-Mannose D-Xylose L-LyxoseWhat prefixes are used in naming the following?(a) A 1,3-disubstituted benzene(b) A 1,4-disubstituted benzene