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fgiga [73]
3 years ago
11

does the nitro group on the pyridine ring make the ring more electron rich or more electron deficient

Chemistry
1 answer:
Arte-miy333 [17]3 years ago
3 0

Answer:

more electron deficient

Explanation:

The nitro group is an electron withdrawing group. It withdraws electrons from the pyridine ring by resonance.

This electron withdrawal by resonance makes the pyridine ring less electron rich or more electron deficient.

Hence, the nitro group makes the pyrinde ring more electron deficient

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Which element is oxidized in the following reaction: 2FeCl₂ + Cl₂→2FeCl₃ if Fe goes from + 2 to +3 and Cl goes from 0 to −2?
Blizzard [7]

Answer:

Fe.

Explanation:

  • The element which is oxidized is the element that losses electrons and its oxidation state be more positive.
  • The element which is reduced is the element that gain electrons and its oxidation state be more negative.

<em> Fe goes from + 2 to +3, so, it is the element that is oxidized.</em>

<em></em>

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3 years ago
How many molecules are in a drop of water weighing 0.05 g?
Scilla [17]

Answer:

0.05 g of H2O contain molecules

7 0
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What makes and acid an acid?
Crank

Answer: The donating of hydrogen ions is what makes an acid an acid. A base, however, is a substance that accepts hydrogen ions.

Explanation:

8 0
4 years ago
The dominant intermolecular force that causes gaseous hcl molecules to attract one another is
AnnyKZ [126]

Answer:

Dipole-dipole attractions

Explanation:

The Cl atom is more electronegative than H, so it attracts the electrons in the H-Cl bond more to itself.

The Cl end of the molecule becomes partially negative (δ-), and the H end becomes more positive (δ+). This separation of charge is called an electric dipole,

When two HCl molecules are near each other, they arrange themselves so that the negative and positive ends of the dipoles line up and attract the two molecules together.

8 0
3 years ago
Draw a Lewis structure for C2H3Cl. Show all unshared electron pairs. None of the atoms bears a formal charge, and all atoms have
aleksklad [387]

Answer:

See picture below

Explanation:

To do this, we first need to know how are the bonds in this molecule are. To do so, let's calculate the number of insaturations in the molecule:

n°I = C+1 - (H-N+X)/2

These numbers indicate if the molecule has double bond, triple bond, ring, cyclo, among other options:

n°I = 3 - (3+1)/2

n°I = 1

As it's a very small molecule, we can assume this molecule only have a double bond, and it's an alkene.

So the lewis structure, shows the electrons and the bonding, and also shows the unshared electron pairs, depending on how much electron have each molecule.

In the case of carbon:

[C] = [He] 2s2 2p2 ----> 4 electrons

[H] = 1s1 ----> 1 electron

[Cl] = [Ne] 3s2 3p5 ----> 7 electrons.

Therefore, we also know that Carbon has a double bond, so, the main molecule would have something like this:

C = C

so next to the carbons, we can put two hydrogens and in the other carbon, the chlorine and the remaining hydrogen.

See picture below for structure:

7 0
3 years ago
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