Chemistry, 05.10.2019 04:20 Kekkdkskdkdk
In the human body, the amino acid phenylalanine is normally processed by an enzyme that converts it to cinnamic acid. infants with phenylketonuria (pku) have a defective enzyme, resulting in a buildup of phenylalanine that can damage a developing brain. people with pku must minimize phenylalanine in their diet by avoiding protein-rich foods and the artificial sweetener aspartame. recent research explores a treatment for pku that uses tiny lipid-bilayer packages called posomes to deliver an alternate enzyme that can convert phenylalanine to cinnamic acid (adv. funct. mater. 2015, 25, 3860- predict the number of signals and the number of protons giving rise to each signal in the h nmr spectra of both phenylalanine and cinnamic acic. enzyme oh nh2 cinnamic acid phenylalanine has the 1h nmr spectrum with signals. signals. cinnamic acid has the 1h nmr spectrum
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Phosphoric acid is a triprotic acid ( =6.9×10−3 , =6.2×10−8 , and =4.8×10−13 ). to find the ph of a buffer composed of h2po−4(aq) and hpo2−4(aq) , which p value should be used in the henderson–hasselbalch equation? p k a1 = 2.16 p k a2 = 7.21 p k a3 = 12.32 calculate the ph of a buffer solution obtained by dissolving 18.0 18.0 g of kh2po4(s) kh 2 po 4 ( s ) and 33.0 33.0 g of na2hpo4(s) na 2 hpo 4 ( s ) in water and then diluting to 1.00 l.
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How do you interpret a chromagram for what mixtures contain?
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In the human body, the amino acid phenylalanine is normally processed by an enzyme that converts it...
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