Leterofunctional compounds Name the following compound: 0 HOOC-C-CH,COOH
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- Drag and drop from the available list of terms. Pair 1 Н H/G₂ C=C CH3CH2 structural H CH3CHCH₂CH₂CH3 1 CH3 optical CH₂CH3 anomers Pair 2 CH3CH2 HC₁ Pair 1 would be classified as isomers, while pair 2 would be classified as isomers. enantiomer undefined C= stereoisomer CH₂CH3 CH3CH₂CHCH₂CH3 I CH3 H cis-trans isotopesAMINO ACIDS 1. Write the tripeptide structure for: val-ser-cys. 2. Write the reactions for: phe + serchiral centers - identify the chiral carbons in the following structures. он Br HO. B OH C ÓH D L and D enantiomers CH2OH CH,OH CH,OH Но -H- H- -OH H- -O- но- H- OH Но- но- H H- OH ČH,OH CH,OH ČH2OH 1. Which, if any, of the carbohydrates above are L-sugars? 2. What makes a molecule an L-sugar rather than a D-sugar? 3. If any of the structures above are not already L-sugars, rewrite the structure to make it into that conformation.
- 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 -OHChoose 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 OHFunctional Group Name Structural Diagram (draw all bonds) Found where in the body??? Hydroxyl -N H Carbonyl #1 (aldehydes)
- Lefer to the figure showing the molecular structure of dimethylmercury. H–C-Hg C-H H. Exposure of human skin to a single drop of dimethylmercury can lead to death, as it is highly poisonous and passes easily cell membranes. Based on its structure, why is it able to pass so easily through cell membranes? I-0-I IICIHOH HO, \OH Starting at the carbon atom marked with the asterisk, and moving around the molecule in a clockwise direction, write down a SMILES string for dexamethasone.compounds? COOH CH,OSO,H но OH OH NH-C-CH, 1) What is/are the major chemical/functional group modifications on these carbohydrates (glycosaminoglycans)? What functions/properties do these modifications impart on the compounds?
- Consider the structure shown below. он 3 5 CH; O CH, O H CH; O 1 H-N-CH,-C-N-CH;-C-N-CH-C-N-CH-C-N-CH-C-ơ 2 H. H H Fill in the blank with an integer (1, 2, 3, 4, 5..) as shown in the diagram or to represent a specified number. A hydrophilic side chain is indicated by the numberwhy does A2-B3 structure is active (contain the antibiotic) and the (A2- B2,A1-B1,A1-B2,A1-B3,A3-B1,A3-B2,A3- B3) are nonactive help please! atorial proce below. A1 A2 A3 N=0 H 2-nitrobenzaldehyde 5-nitro-2-furaldehyde 3-nitrobenzaldehyde B1 B2 NH₂ HN. 4-bromophenylhydrazine hydrochloride B3 NH₂ Br HN. 4-cyanophenylhydrazine hydrochloride NH₂ HN CẠNH NH₂ aminoguanidine bicarbonateII. Arrange the following compounds in order of increasing: A. boiling point B. acidity C. solubility. Explain your arrangement. OH HO OH 1. 2. Octan-1-ol 3. II. Given the following: OH OH HO, A в 1. Provide the alkene needed to synthesize each of the compounds given by oxymercuration- demercuration. 2. Provide the alkene needed to synthesize each of the compounds given by hydroboration- oxidation.