What is the complete name of the following sugar? но он носн OH Write out the words alpha and beta. This question is case-sensitive. Capitalize only the configuration designation, D or L, example: beta D-glucopyranose.
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A: Disaccharides are sugar formed by joining two monosaccharides by glycosidic linkage. Some examples…
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Q: at is the pyranose/furanose ring structure of this sugar?
A:
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A: A Haworth projection is a common way of writing a structural formula to represent the cyclic…
Q: what is the name of the monosaccharide A?
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Q: H2N H -N Orcinol но A но он
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Q: Draw the Hayworth projection for a furanose and pyranose form of D-talose. сно -H -H H- HO- ČH2OH
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A: REDUCING SUGAR: A sugar molecule which can undergo chemical reactions like oxidation by acting as a…
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Q: O-a-D-glucopyranosyl-(1→1)- a-D-glucopyranoside
A:
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Q: Complete the following table by providing the Fischer and Haworth Projections of the given sugars.…
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A: it is a nucleotide because it has a sugar a nitrogenous base and a phosphate group.
Q: 4.) C-3 epimer of Fructose
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Q: Draw the Fischer projection for a monosaccharide.
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- Complete the following table by providing the Fischer and Haworth Projections of the given sugars. (Please be careful with the alpha and beta, and the complete and abbreviated) (not a graded question) Sugar Fischer Projection Haworth Projection (Complete) alpha-anomer Haworth Projection (Abbreviated) beta-anomer L-Galactose L-FructoseWhat structural relationship is indicated by the term D-sugar? Why are (+) glucose and (-) fructose both classified as D-sugars?Why 14C@phenylalanine is used ?
- 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- XyloseComplete 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-LyxoseAll naturally occurring polysaccharides have one terminal residue, which contains a free anomeric carbon. Why do these polysaccharides not give a positive chemical test for a reducing sugar?Please explain
- 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-Mannose D-Xylose L-Lyxoseis this an alpha or beta sugar? How can you tell?As a substituent, the hydrocarbon “tail” of the Ibuprofen molecule (see circle above) can be best described as n-butyl.  sec-butyl. isobutyl. tert-butyl