Drag and drop from the available list of terms.Pair 1НH/G₂C=CCH3CH2structuralHCH3CHCH₂CH₂CH31CH3opticalCH₂CH3anomersPair 2CH3CH2HC₁Pair 1 would be classified asisomers, while pair 2 would be classified asisomers.enantiomerundefinedC=stereoisomerCH₂CH3CH3CH₂CHCH₂CH3ICH3Hcis-transisotopes

Isomers -isomers are molecules which have same molecular formula but differ in the arrangements of…

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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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Determine the number of possible stereoisomers for the fol- lowing compounds: CH,OH C=0 CH,OH Но-с—н C=0 H-C-OH H-C-OH H-C-OH H-C-OH H-C-OH CH,OH CH,OH Ribulose Sedoheptulose
Draw the enantiomer structure of the following given carbohydrates. Be sure to include appropriate D or L specification.
In the space provided, draw a Haworth projection for the beta anomer of the following monosaccharide Fischer projection. CHO HO-C-H HO-C-H HO-C-H H-C-OH CH,OH
Differences between Cis-fatty acid VS. Trans fatty acids Limit your answer to two sentences only to every question. Copy and complete the table. GIVEN: DRAW THE EXPANDED STRUCTURE NAME THE BONDS [Molecular Orbitals &Hybrid Orbitals] IUPAC NAME CHOOSE THE SIMPLEST Unsaturated FATTY ACID NAME OF THE COMPOUND Cis-fatty acid Trans-fatty acid
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
Choose the correct structure for thiamine hydrochloride at pH 3. H3C H3C NH₂ NH₂ 'N CI- A CI- с CH3 CH3 S HCI OH N NH3 H3C N H3C CI- B NH₂ CH3 ** N CH3 D HCI -OH OH
Draw one aromatic polar amino acid at pH 7. Label with full name, three letter abbreviation, and single letter symbol.
NH3* *H3N Give the abbreviation for the above tripeptide using the three-letter codes for each amino acid. Z-エのエ-Z
Following are Fischer projections for a group of five-carbon sugars, all of which are aldopentoses. Identify the pairs that are enantiomers. CHO сно H-C- OH H-C-OH H-C- OH но-с — н н-с—он но- ČHOH ČH,OH сно CHO Н-с—он но—с— н H-C- OH H-C-OH но—с—н Н-с—он ČHOH ČH,OH сно сно н-с—он но—с —н но—с— н но -с — н H-C- OH но- C-H ČH,OH ČH,OH
Classify each structure as D or L.
In the following monosaccharide hemiacetal, identify the anomeric carbon atom. Identify the appropriate atom by selecting an atom and assigning it a map number of 1. To do this, rigl mark to enable the Map field before entering a value. H: 122 EXP" CONT. 0 0 H но OH S Br OH [1] ÓH P. -
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

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Drag and drop from the available list of terms. Pair 1 c= CH3CH₂ H CH₂CH3 Pair 2 CH3CHCH₂CH₂CH3 T CH3 H c= CH3CH2 CH₂CH3 H CHỊCH, CHCH CHS CH3 Pair 1 would be classified as isomers while nair 2 would be classified as