Radioactive decay => C = Co { e ^ (- kt) |
Data:
Co = 2.00 mg
C = 0.25 mg
t = 4 hr 39 min
Time conversion: 4 hr 39 min = 4.65 hr
1) Replace the data in the equation to find k
C = Co { e ^ (-kt) } => C / Co = e ^ (-kt) => -kt = ln { C / Co} => kt = ln {Co / C}
=> k = ln {Co / C} / t = ln {2.00mg / 0.25mg} / 4.65 hr = 0.44719
2) Use C / Co = 1/2 to find the hallf-life
C / Co = e ^ (-kt) => -kt = ln (C / Co)
=> -kt = ln (1/2) => kt = ln(2) => t = ln (2) / k
t = ln(2) / 0.44719 = 1.55 hr.
Answer: 1.55 hr
Answer:
A.
Explanation:
The <u>tertiary structure </u>of proteins is related to the interactions between the amino acids of the <u>primary structure</u>. Thus, these interactions give it a specific three-dimensional configuration which is very sensitive to <u>functionality</u>.
For example, <u>allosteric inhibitions</u> are related to this concept. When the <u>inhibitor</u> changes the tertiary structure of the protein it loses all <u>activity</u> and for the catalysis of the reaction.
Thus, the primary structure (which is related to the specific <u>sequence of amino acids</u>) will determine the tertiary structure since the chain folds will be a consequence of<u> intra-amino acid interactions</u>.
Answer:
Four possible isomers (1–4) for the natural product essramycin. The structure of compound 1 was attributed to essramycin by 1H NMR, 13C NMR, HMBC, HRMS, and IR experiments.
Explanation:
Three synthetic routes were used to prepare all four compounds (Figure 2A). All three reactions utilize 2-(5-amino-4H-1,2,4-triazol-3-yl)-1-phenylethanone (5) as the precursor, whereas each uses different esters (6–8) to construct the pyrimidinone ring. Isomer 1 was prepared by reaction A, which used triazole 5 and ethyl acetoacetate (6) in acetic acid. This was the reaction used in syntheses of essramycin by the Cooper and Moody laboratories.3,4 Reaction B produced compound 2 (minor product) and compound 3 (major product), which were separated chromatographically. This reaction allowed reagent 5 to react with ethyl 3-ethoxy-2-butenoate (7) in the presence of sodium in methanol, under reflux for 24 h. Compound 4 was prepared by reaction C, which was obtained by reflux of 5 and methyl 2-butynoate (8) in n-butanol.
Change in velocity over time is acceleration.
You're finding acceleration .
Yes because the protons are the same but the neutrons change