Yes. It is element No. 8 on the periodic table.
Answer:
50 because it’s a ratio problem
Explanation:
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:
Only one—(i), or (ii), or (iii)—increases the reaction rate.
Explanation:
<em>Which of the following changes always leads to an increase in the rate constant for a reaction?</em>
- <em>Decreasing the temperature. </em>NO. A lower temperature leads to a slower reaction because the molecules have less energy to react.
- <em>Decreasing the activation energy</em>. YES. According to the Arrhenius equation, the lower the activation energy, the higher the rate constant.
- <em>Making the value of ΔE more negative</em>. NO. A more negative ΔE means a reaction is more spontaneous but not faster.