H. N-C-C H' R H, N-C-C O-H HO H. N-C-C-N-C-C O-H R R. HR Using the graphic above answer the following questions. Please correctly identify the molecule above. Correctly name its monomer. Correctly name its polymer. H-U
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Q: NUCLEIC ACID "BASE PAIRING" 1. 5'-A-T-A-A-G-G-G-G-C-T-C-3' 2. 5'-G-G-G-G-C-T-A-C-T-C-3'
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Q: Match the monomer with the biological molecule
A: Monosaccharide - Carbohydrate Amino acids - Protein
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- Please clearly identify each numbered amino acid side chain, below. Your description should include the name or 3 letter code for the amino acid and the type (i.e., chemical class) of the amino acid. 1 4 OH OH CH, CH, CH2 CH2 CH, "H,N-C-C-0 "H,N-C-C-0 "H,N-C-C-0 _0-5-5-N H. H O H O HO ноIndicate 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!Which of the following peptides will likely form an irregular structure? A-D-I-E-L-Y-F-H-I-C-V-D-E A-R-E-G-H-Y-D-G-C-Q-S-G A-R-E-V-H-Y-D-I-C-Q-S-F A-R-E-F-C-Y-D-I-C-Q-S-P
- Identify the chiral carbons in -D-fructose. Identify the appropriate atom by selecting an atom and assigning it a map number of 1. To do this, ri mark to enable the Map field before entering a value. EXP. CONT. но- S CI Br ÓH ÓH P F z OIdentify the biomolecule represented by the following image. O=P-O. 5' Base ОН 4" 1' 3 2' ОНSelect the incorrect statement(s). CH₂ OH NH₂ Polypeptide backbone CH₂ A C- CH₂ CH CH3 CH3 CH3 CH3 CH CH₂ NH₂ CH₂ CH₂ CH₂ CH₂ B D This is a tertiary structure of a protein. Letter A represents hydrogen bond. Letter C represents disulfide bond. This represents a secondary structure. This illustrates a quaternary structure.
- T/F: The titration curve for serine will have 2 inflection points. T/F: The Amino Acid D-selenocysteine has an R-Configuration T/F: Each water molecule can form H bonds with 4 other water molecules T/F: In a buffer system, decreasing the concentration of the conjugate base relative to acid makes the buffer more acidic T/F: Glycine forms good interactions in a protein structure True or false?-s/67365/take The image below shows the structure of a lipid. Which of the following statement is correct about the lipid shown in the image Stearic acid ННННННННННННННННН .................. Н-С-О-c-c-c-с-с-с-с-с-с-с-с-с-с-с-с-с-с-с-н Н Carboxylic acid group 10 glycerol ................. ННННННННННННННННН Онн .... H-C-0-c-c-c-c-c-c-c=С-С-С=С-С-С-С-С-С-c-С-Н ................ НННННННННННННННН НННННН | | | | | ОННННН ...... ns://canvas uts edu au/accoccmont Н-С-О-c-c-c-c-c-c-c=c-c-c=c-c-c-c-c-c-c-c-н |--1.... ... ... ... НННННННННННННННН hrefr | Н 5.000 (1 ННННННН |||||| Linoleic acidH HN-C-C-OH H-C-CH, CH2 CH3 The following short passage is about the compound with chemical structure shown above. Use the following word bank to fill in the blanks in the passage. NOTE that some options may be used more than once: functional, L-serine, nonpolar, two, carboxyl, ketone, optimally, hydroxyl, three polar, neutral, methyl, L-isoleucine, four, amino, carbonyl, L-threonine, acidic, one, aldehyde, hydroxide, amine, D-threonine, asymmetrical, optically, D-serine basic, D-isoleucine, 2-hydroxybutanoic acid, L-glutamic acid, five, ionisable active compound with a maximum number of chiral carbon(s) Its is an example of a(n) chemical structure also contains a maximum number of ionisable group(s) at physiological pH. While the presence of a(n) group gives the compound its partial acidic properties group makes this compound nonpolar, the presence of a(n)
- 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 IICIHGiven the following monosaccharide, draw both the given monosaccharide and the enantiomer. Do not use R in your answer. CHO H- HO H- H. HO- ČH,OH SearchMass spectrometry and X‑ray diffraction are common biochemical techniques for characterizing proteins. Classify each statement based on whether it applies to mass spectrometry, X‑ray diffraction, or both techniques.