some regions of a polypeptide may coil or fold back on themselves. this is called <u>secondary structure</u> , and the coils or folds are held in place by <u>hydrogen bonds</u>
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After translation, primary structure is just the arrangement of amino acids. The interactions between the carbonyl, amino, and side groups of the amino acid polymer backbone inside the chain result in the secondary structure of proteins. These interactions are primarily fueled by hydrogen bonds, which result in the formation of alpha helices and beta sheets, which are the primary features of proteins' secondary structures.
To create a useful three-dimensional structure, tertiary structure requires more interactions within the protein chain. Disulfide bonds between cysteines, hydrophobic contacts, ionic bonding, and dipole-dipole interactions are a few of these interactions. To create a useful, three-dimensional protein structure, several protein chains interact in quaternary structure.
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Answer:
0.8 g/cm^3
Explanation:
Density is the amount of substance present per volume.
Density = Mass / Volume = (25.0 g) / (30.0 cm) = 0.83333 g/cm^3
=> Density = 0.8 g/cm^3 (rounded up to one decimal place)
It's about .0934 Liters at STP.
Answer:
It basically messes up the results
Explanation:
Pen ink consists of resins, pigments and other colouring dyes dissolved in appropriate solvents like propylene glycol, propyl alcohol and some other ethers. If the ball point pen is used to mark on the chromatography paper then these pigments will also move along with the solvent and interfere with the spots of our analyte.
If you use a ball point pen when doing a chromatogram, then the ink would separate as it is a mixture and run down the paper.
Graphite, or pencil lead however, is not an organic material and therefore will not be affected by common organic solvents used for thin-layer chromatography. Pen ink on the other hand will be readily absorbed by the solvent and will move up the plate.
