The three major groups on the peridoic table are the ____

Chemistry

1 answer:

qaws [65]3 years ago

5 0

Metals on the left side, metalloids on the staircase, nonmetals on right side

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Draw the best Lewis structure for NH3 by filling in the bonds, lone pairs, and formal charges. (Assign bonds, lone pairs, radica

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Answer : The Lewis-dot structure of $NH_3$ is shown below.

Explanation :

Lewis-dot structure : It shows the bonding between the atoms of a molecule and it also shows the unpaired electrons present in the molecule.

In the Lewis-dot structure the valance electrons are shown by 'dot'.

The given molecule is, $NH_3$

As we know that hydrogen has '1' valence electron and nitrogen has '5' valence electrons.

Therefore, the total number of valence electrons in $NH_3$ = 5 + 3(1) = 8

According to Lewis-dot structure, there are 6 number of bonding electrons and 2 number of non-bonding electrons.

Now we have to determine the formal charge for each atom.

Formula for formal charge :

$\text{Formal charge}=\text{Valence electrons}-\text{Non-bonding electrons}-\frac{\text{Bonding electrons}}{2}$

$\text{Formal charge on N}=5-2-\frac{6}{2}=0$

$\text{Formal charge on }H_1=1-0-\frac{2}{2}=0$

$\text{Formal charge on }H_2=1-0-\frac{2}{2}=0$

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What compound is formed when 2,2-dimethyloxirane (2-methyl-1,2-epoxypropane) is treated with ethanol containing sulfuric acid

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On this reaction, we have an "epoxide" (2-methyl-1,2-epoxypropane). Additionally, we have acid medium (due to the sulfuric acid $H_2SO_4$ ). The acid medium will produce the hydronium ion ( $H^+$ ). This ion would be attacked by the oxygen of the epoxide. Then a carbocation would be produced, in this case, the most stable carbocation is the tertiary one. Then an ethanol molecule acts as a nucleophile and will attack the carbocation. Finally, a deprotonation step takes place to produce 2-ethoxy-2-methylpropan-1-ol.