Answer:
The fraction of energy used to increase the internal energy of the gas is 0.715
Explanation:
Step 1: Data given
Cv for nitrogen gas = 20.8 J/K*mol
Cp for nitrogen gas = 29.1 J/K*mol
Step 2:
At a constant volume, all the heat will increase the internal energy of the gas.
At constant pressure, the gas expands and does work., if the volume changes.
Cp= Cv + R
⇒The value needed to change the internal energy is shown by Cv
⇒The work is given by Cp
To find what fraction of the energy is used to increase the internal energy of the gas, we have to calculate the value of Cv/Cp
Cv/Cp = 20.8 J/K*mol / 29.1 J/K*mol
Cv/Cp = 0.715
The fraction of energy used to increase the internal energy of the gas is 0.715
Answer:
324.18 g/mol
Explanation:
Let the molecular mass of the antimalarial drug, Quinine is x g/mol
According to question,
Nitrogen present in the drug is 8.63% of x
So, mass of nitrogen = 
Also, according to the question,
2 atoms are present in 1 molecule of the drug.
Mass of nitrogen = 14.01 amu = 14.01 g/mol (grams for 1 mole)
So, mass of nitrogen = 14.01×2 = 28.02
These 2 must be equal so,

solving for x, we get:
<u>x = 324.18 g/mol</u>
Answer:
= 12 mL H202
Explanation:
Given that, the concentration of H2O2 is given antiseptic = 3.0 % v/v
It implies that, 3ml H2O2 is present in 100 ml of solution.
Therefore, to calculate the amount of H202 in 400.0 mL bottle of solution;
we have;
(3.0 mL/ 100 mL) × 400 mL
= 12 mL H202
It matches the universal pH indicator and is indicating the proper pH
Complete question from other source attached
Answer:
Explanation:
Catalyzed by DNA polymerase - both. DNA polymerase catalyzes DNA replication in the cell. However, purified versions of the enzyme are also used to synthesise DNA as part of PCR reactions
involves leading strand synthesis only - PCR. In PCR, lagging strand synthesis is not carried out because the DNA is denatured (rendered single stranded). Therefore, each strand is replicated independently by leading strand synthesis
duplicates a small fragment of the genome - PCR. Usually, to carry out PCR, small sequences called primers are used that specify the region of DNA to be replicated
duplicates the entire genome - in vivo replication - when the DNA is replicated in vivo, the entire genome is replicated. This is carried out prior to cell division so that two daughter cells can each inherit a copy of the entire genome