Naming and drawing cyclic monosaccharides Give the complete common name, including anomer and stereochemistry labels, of the following molecules. You will find helpful information in ALEKS Data resource. CH2OH OH H H OH H H OH H OH HOCH2 OH OH H H CH₂OH H OH HOCH2 OH H OH D H H OH H HOCH2 CH, OH H H H OH OH OH Explanation Check α B Y x G Even Muxiam Hill LLC. All Rights Reserved. Terms of Use | Priv

Naming and drawing cyclic monosaccharides Give the complete common name, including anomer and stereochemistry labels, of the following molecules. You will find helpful information in ALEKS Data resource. CH2OH OH H H OH H H OH H OH HOCH2 OH OH H H CH₂OH H OH HOCH2 OH H OH D H H OH H HOCH2 CH, OH H H H OH OH OH Explanation Check α B Y x G Even Muxiam Hill LLC. All Rights Reserved. Terms of Use | Priv

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

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f) Alkene X can be decomposed with hydrogen peroxide catalyzed by sodium tungstate to substance Q. This can be further degraded by iodoform reaction to substance R. Give the structures of substances Q and R. Xx S Na₂WO4 H₂O2 Q (C9H1603) 1: NaOH, 1₂ 2: H+ P₂O5 teplo - CHI3 R (C8H1404) P₂O5 teplo T g) The preparation of substance Q from substance X using hydrogen peroxide is a redox reaction. Identify the reductant and oxidant in this reaction, write the formal oxidation number to the atoms where it changes during the reaction and calculate the reaction. h) Substances Q and R undergo a reaction with phosphorous oxide under heating to form various products T and S. Determine the structure of substances T and S if you know their H NMR : 1H NMR (S): 2.2 (t, 2H); 1.8 (t, 2H); 1.3 (s, 6H). 1H NMR (T): 4.6 (d, 1H); 4.3 (d, 1H); 2.2 (t, 2H); 1.5 (t, 2H); 1.3 (s, 6H).
Provide an IUPAC name for each of the compounds shown. (Specify (E) (Z) stereochemistry, if relevant, for straight chain alkenes only. Pay attention to commas, dashes, etc.) CH3 CH3 1.) -CH2CH3 CH2CH3 2.)
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Dienes, Aromaticity, EAS, NAS 1. Give a systematic name for each of the following structures. Indicate relevant stereochemistry if present. NH₂
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Predict the organic products of the reaction. Show stereochemistry clearly. Draw the products according to the specified (R) or (S) designation for each stereocenter carbon atom. H 1) OsO4, pyridine 2) Na,SO3 or NaHSO; in H, O organic products