<u>Answer:</u>
<em>The situation given here is imaginary such that the life of Rock has to be found using the half-life of the element lokium that has been found inside the rock. </em>
<u>Explanation:</u>
Half-life of any material is the amount of time taken by that particular material to decay. Now the amount of lokium found in rock can show after how many half-lives this amount has been left out.
The time elapsed will be log (L) atoms X half-life.
Answer:
<em>What can be added to an atom to cause a nonvalence electron in the atom to temporarily become a valence electron </em>is<u><em> energy</em></u><em>.</em>
Explanation:
The normal state of the atoms, where all the electrons are occupying the lowest possible energy level, is called ground state.
The <em>valence electrons</em> are the electrons that occupy the outermost shell, this is the electrons in the highest main energy level (principal quantum number) of the atom.
So, a <em>nonvalence electron</em> occupies an orbital with less energy than what a valence electron does; in consequence, in order to a nonvalence electron jump from its lower energy level to the higher energy level of a valence electron, the former has to absorb (gain) energy.
This new state is called excited state and is temporary: the electron promoted to the higher energy level will emit the excess energy, in the form of light (photons), to come back to the lower energy level and so the atom return to the ground state.
1 is b 2 is a 3 is d 4 is a 5 is c
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.
A volcano is created when hot molten rock, ash and gases escape from an opening in the Earth's surface. The molten rock and ash solidify as they cool, forming the distinctive volcano shape shown here. As a volcano erupts, it spills lava that flows downslope. Hot ash and gases are thrown into the air.
