What type of reaction is shown below?

1 answer:

8 0

An exothermic reaction is a type of chemical reaction in which energy is released to the environment in form of heat or light. Endothermic reaction in the other hand is a chemical reaction where energy is taken from the surroundings and thus the surroundings end up with less energy than they started with. In this case; the above reaction is an Exothermic reaction (heat is being released to the surroundings).

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The bond type in CaO is

sergey [27]

CaO is an ionic bond

4 0

3 years ago

Pharmacists sometimes measure medicines in the unit of "grains," where 1 gr = 65 mg. The label on a bottle of aspirin reads "Asp

viva [34]

Answer:

325mg of Aspririn

Explanation:

First you should note the information that the problem gives you:

- The bottle of Aspirin has 5gr (grains)

- 1gr(grain) = 65mg (miligrams)

Also, the problem is asking about how many aspirin are in 5 gr (grains), so you should use a conversion factor, as follows:

-First you should put the quantity you need to convert:

$5grAspirin$

-Then you write the denominator of the conversion factor that must have the same units that you want to convert, in this case gr:

$5grAspirin*\frac{}{1grAspirin}$

-Then you write the numerator with the units that you want to obtain and the numerical equivalence between the units, in this case:

$5grAspirin*\frac{65mgAspririn}{1grAspirin}$

-Finally you multiply numerators and divide by denominators:

$5grAspirin*\frac{65mgAspririn}{1grAspirin}=325mgAspririn$

8 0

3 years ago

10. Isolation of a pure sample of the third product, which has been determined to be an isomer of the major and minor products,

Ymorist [56]

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.