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VMariaS [17]
3 years ago
13

What happend to the pressure of a gas inside a container if the temperatures of the gas decreases

Chemistry
1 answer:
ludmilkaskok [199]3 years ago
4 0
There is an increase in the number of collisions between particles and the walls of the container<span>. b. There is an increase in the </span>temperature of the gas. If<span> the volume of a </span>container<span> of </span>gas<span> is reduced, what will </span>happen to the pressure inside<span> the </span>container
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3. Hydrogen reacts with nitrogen to produce ammonia according to the equation:
lys-0071 [83]

Mass of ammonia produced : 121.38 g

<h3>Further explanation</h3>

Given

Reaction

3H₂(g) + N₂(g) ⇒ 2NH₃(g)

100g of N₂

Required

Ammonia produced

Solution

mol of N₂ :

\tt mol=\dfrac{mass}{MW}\\\\mol=\dfrac{100}{28}\\\\mol=3.57

From the equation, mol ratio of N₂ and NH₃ = 1 : 2, so mol NH₃ :

\tt \dfrac{2}{1}\times 3.57=7.14~moles

mass of NH₃(MW=17 g/mol) :

\tt mass=mol\times MW\\\\mass=7.14\times 17\\\\mass=121.38~g

8 0
3 years ago
How many moles of copper are present in a sample that contains 4.55 x 10^24 atoms of copper
FinnZ [79.3K]

Hope you could understand.

If you have any query, feel free to ask.

3 0
2 years ago
What would be the best way to measure the volume of a small ?​
WITCHER [35]
You can use a graduated cylinder.
6 0
3 years ago
PLEASE ANSWER FAST!!!!!!!!!!!!!!!
Savatey [412]

Answer:

The answer is A. a wave of vibrating electric and magnetic energy.

6 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.

7 0
3 years ago
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