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AnnZ [28]
3 years ago
14

Why were they put into water before we tested them?

Chemistry
2 answers:
klasskru [66]3 years ago
7 0

explain the question your asking

gtnhenbr [62]3 years ago
3 0

we dont know what they put in the water

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A 1.25 g gas sample occupies 663 ml at 25∘ c and 1.00 atm. what is the molar mass of the gas?
lakkis [162]

Using ideal gas equation,  

P\times V=n\times R\times T

Here,  

P denotes pressure  

V denotes volume  

n denotes number of moles of gas  

R denotes gas constant  

T denotes temperature  

The values at STP will be:  

P=1 atm  

T=25 C+273 K =298.15K

V=663 ml=0.663L

R=0.0821 atm L mol ⁻¹

Mass of gas given=1.25 g g

Molar mass of gas given=?

Number of moles of gas, n= \frac{Given mass of the gas}{Molar mass of the gas}

Number of moles of gas, n= \frac{1.25}{Molar mass of the gas}

Putting all the values in the above equation,

1\times 0.663=\frac{1.25}{Molar mass of the gas}\times 0.0821\times 298.15

Molar mass of the gas=46.15

3 0
3 years ago
The elements least likely to form bonds are found in which group? 15, 16, 17, 18
Ipatiy [6.2K]

Answer:

D.18

Explanation:

Edgenuity

3 0
3 years ago
Read 2 more answers
The decay of radioisotopes is a typical first order reaction. The half-life of carbon-14 (14C) is a radioactive isotope that dec
Nady [450]

Answer:

By emitting an electron and an electron antineutrino, one of the neutrons in the carbon-14 atom decays to a proton and the carbon-14 (half-life of 5,700 ± 40 years) decays into the stable (non-radioactive) isotope nitrogen-14.

Half-life: 5,730 ± 40 years

Names: carbon-14, C-14, radiocarbon

Isotope mass: 14.003241 u

8 0
3 years ago
The loss of one or more electrons from an atom is called
snow_tiger [21]
Loss of an electron is oxidation! 
6 0
3 years ago
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Diazomethane is a toxic yellow gas that is both sensitive and explosive. However, it is a useful reagent in the laboratory to ma
Alona [7]

Answer:

Carboxylic acids react with diazomethane to produce methyl esters.

Explanation:

Diazomethane has a high reactivity and is used to produce methyl esters with carboxylic acid in a immediately reaction, carried out at room temperature in the absence of catalysts.

As we can see in the image below

  • In the First Step, occurs an acid-base reaction to obtain the "carboxylate" ion.
  • Second Step: The Carboxylate attacks the protonated diazomethane by a SN2 reaction to<u> finally get the Methyl Ester.</u>

The subproduct is Nitrogen; knowing this, we must be careful with the production of this gas, and do the process in a vented place

4 0
4 years ago
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