Look at the structure of the disaccharide shown. Name the type of bond which is present.CH,OHHHонноCH2ОнHонHÓHO B - 1, 4- N-glycosidic linkageO a- 1, 4- O-glycosidic linkageO B- 1, 4-0-glycosidic linkageO a- 1, 6- 0-glycosidic linkageO a- 1, 4- N-glycosidic linkage

Disaccharides exist in more than one chemical conformational structure. The alpha and beta forms of…

Answered: Look at the structure of the…

Biochemistry

9th Edition

ISBN:9781319114671

Author:Lubert Stryer, Jeremy M. Berg, John L. Tymoczko, Gregory J. Gatto Jr.

Publisher:Lubert Stryer, Jeremy M. Berg, John L. Tymoczko, Gregory J. Gatto Jr.

Chapter1: Biochemistry: An Evolving Science

Section: Chapter Questions

Problem 1P

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Give the systematic name of the the disaccharide shown below: CH2OH CH2OH H H Н ОН Н Н ОН Н H H ОН H. ОН H ОН
An incomplete structure of a porphyrin ring is shown below. The structure is missing three pi bonds and does not show the non-zero formal charges on two atoms. Complete the structure of the porphyrin ring with the missing pi bonds and formal charges. 0 0 +t DC 12⁰ H C N O S F P Cl Br I
Identify the functional groups in the following compounds
CH;OH НО OH What is the name of this structure? OH OH alpha-D-gulopryranose O beta-L-gulofuransone O alpha-L-gulofuranose beta-D- gulopyranose
A)Label each sugar as D or L b. Label each sugar as a or B
Indicate next to each letter the name of the monomers shown below and write the name of the polymer that is produced from the monomer. H-C-OH HỌ-C-H H-C-OH H-C-OH о- 6 CH₂OH 0=P-O О CH₂ Phosphate H group А: Name of polymer: H- Н Н OH H Sugar Н Н. H Nitrogenous base (adenine) C: 0 НО Name of polymer: H C-C-N CH2 SH Н НИ Н III H-N-С-С-0 +111 НКН н B: Name of polymer: Н 0 0-C-H o Н-С-0² H-C-O H S ННННННННННН Н Н Н LI -CH Н ННННННННННН Н Н Н ITIILE I C-C H ...... С-с-с-с-с-с-с III E .. ННННННННННН Н Н С-С-f 111 1 FE D: I НННННННННННННН No polymer!
Although the first two carbons of fructose and glucose are identical in structure to DHAP and GADP (from glycolysis), DHAP and GADP equilibriate on their in solution to favor the ketone over the aldehyde, while fructose and glucose do not. Why? a)The larger size of the molecule sterically hinders the isomerization b)The larger sugars have more OH groups which hydrogen bond and disrupt isomerization c)The larger sugars cyclize, and there is no carbonyl to isomerize in the cyclic form d)The larger sugars cyclize, and in the cyclic form the hydrogen bonding is very strong e)The larger sugars are less soluble in water than the smaller sugars
Explain these diagrams
Choose the correct structure for thiamine hydrochloride at pH 10. H3C H3C N NH₂ NH₂ CI- A CI- с CH3 CH3 HCI -OH OO H3C H3C N NH3 NH₂ CI- B D CH3 S CH3 S HCI OH -OH
Explain the structure and its components
Name the types of glycosidic bonds found in this olygomer, from left to right (from 1 to 3) CH 20H CH 2OH CH 2OH но OH OH OH OH OH OH O alpha1-1, alpha1-4, n O alpha1-4, alpha1-4, n O alpha1-4, beta1-2 O alpha1-4, beta1-4 O beta1-4, alpha 1-4 « Previous Next Not saved Submit Quiz
Name the nitrogenous bases that are bonded

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Look at the structure of the disaccharide shown. Name the type of bond which is present. CH2OH H он он CH2 H он H ÓH ÓH O B - 1, 4- N-glycosidic linkage O a- 1, 4- 0-glycosidic linkage O B- 1, 4-0-glycosidic linkage O a- 1, 6- O-glycosidic linkage O a- 1, 4- N-glycosidic linkage