Answer:
See figure 1
Explanation:
On this case we have a <u>base</u> (methylamine) and an <u>acid</u> (2-methyl propanoic acid). When we have an acid and a base an <u>acid-base reaction </u>will take place, on this specific case we will produce an <u>ammonium carboxylate salt.</u>
Now the question is: <u>¿These compounds can react by a nucleophile acyl substitution reaction?</u> in other words <u>¿These compounds can produce an amide? </u>
Due to the nature of the compounds (base and acid), <u>the nucleophile</u> (methylamine) <u>doesn't have the ability to attack the carbon</u> of the carbonyl group due to his basicity. The methylamine will react with the acid-<u>producing a positive charge</u> on the nitrogen and with this charge, the methylamine <u>loses all his nucleophilicity.</u>
I hope it helps!
Answer : The fugacity in the solution is, 16 bar.
Explanation : Given,
Fugacity of a pure component = 40 bar
Mole fraction of component = 0.4
Lewis-Randall rule : It states that in an ideal solution, the fugacity of a component is directly proportional to the mole fraction of the component in the solution.
Now we have to calculate the fugacity in the solution.
Formula used :

where,
= fugacity in the solution
= fugacity of a pure component
= mole fraction of component
Now put all the give values in the above formula, we get:


Therefore, the fugacity in the solution is, 16 bar.
Fluorine is a nonmetal and as such it would need to take in or obtain an electron from a metal to have a stable octet, or full number of 8 electrons in its valence shell. Thus due to the indifference of electrons and protons it becomes an anion, a negatively charged ion.
Answer:
Wouldn't the Earth's atmosphere be moving too fast that it eventually breaks out?
Explanation:
Do NOT trust me.