Answer:
N,N-dimethylacetamide is formed.
Explanation:
- It is an example of a nucleophilic addition-elimination reaction. Here dimethylamine acts as a nucleophile.
- In the first step, dimethyl amine gives nucleophilic addition reaction at carbonyl center of acetyl chloride.
- In the second step, removal of Cl atoms occurs.
- In the third step, deprotonation takes place from amino group to produce N,N-dimethylacetamide.
- Full reaction mechanism has been shown below.
Answer:
Because of its weak intermolecular forces.
Explanation:
Hello there!
In this case, according to the given description, it turns out possible for us to recall the chemical structures of both ethanol and dimethyl ether as follows:

Thus, we can see that ethanol have London dispersion forces (C-C bonds), dipole-dipole forces (C-O bonds) and also hydrogen bonds (O-H bonds) which make ethanol a liquid due to the strong hydrogen bonds. On the other hand, we can see that dimethyl ether has just London and dipole forces, which are by far weaker than hydrogen bonding, that makes it unstable when liquid and therefore it tends to vaporize quite readily.
Regards!
<em><u>ANSWERS</u></em><em><u> </u></em><em><u>:</u></em><em><u>-</u></em>
<em>1</em><em>)</em>

<em>2</em><em>)</em>

<em>3</em><em>)</em>
<em>
</em>
<em>4</em><em>)</em>
<em>
</em>
<em>5</em><em>)</em>
<em>
</em>
<em>(</em><em>mark</em><em> </em><em>me</em><em> </em><em>brainliest</em><em> </em><em>please</em><em> </em><em>I</em><em> </em><em>need</em><em> </em><em>3</em><em> </em><em>more</em><em> </em><em>:</em><em>)</em><em>)</em>
<em>
</em>
Answer:
Dense materials sank into the core and the lighter materials rose toward the surface.
Answer:
Solar winds do not reach well beyond our planet
Explanation:
I hope this helps :)