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:
3
Explanation:
The first election shell can only hold 2 electrons, but the next one can hold up to 8
Answer:Noble gases:
are highly reactive.
react only with other gases.
do not appear in the periodic table.
are not very reactive with other elements.
Explanation:Noble gases:
are highly reactive.
react only with other gases.
do not appear in the periodic table.
are not very reactive with other elements.
Viscosity is the rate at which liquids flow.
Answer:
B. 1-Butene rightarrow (1) BH3: THF (2)H202, OH-
Explanation:
In the hydroboration of alkenes, an alkene is hydrated to form an alcohol with anti-Markovnikov orientation.
the reagent BH₃:THF is the way that borane is used in organic reactions. The BH₃ adds to the double bond of an alkene to form an alkyl borane. Peroxide hydrogen in basic medium oxidizes the alkyl borane to form an alcohol. Indeed, hydroboration-oxidation converts alkenes to alcohols by adding water through the double bond, with anti-Markovnikov orientation.