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Eddi Din [679]
3 years ago
6

I need help with this

Chemistry
1 answer:
son4ous [18]3 years ago
4 0

Answer:

2nd one

Explanation:

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You collect 44.8 L of ammonia in excess hydrogen (N=14amu,H=1amu) . For the Haber process, N2+3H2â2NH3 , what volume of nitrogen
garik1379 [7]

Answer:

d

Explanation:

Firstly, we need to see the theoretical mole ratio between nitrogen and ammonia from the balanced chemical equation. This is 1 to 2. One mole of nitrogen yielded two moles of ammonia.

At STP, one mole of a gas occupies a volume of 22.4, hence we need to know the volume occupied by a volume of 44.8L of ammonia. This is equal to 44.8/2 = 2 moles

Now we have seen the actual number of moles of ammonia yielded. Since this is the same as the theoretical, it means that only one mole of nitrogen was also used up.

Since it is one mole, the volume at STP is thus 22.4L

4 0
4 years ago
What factors mechanical weathering ?. <br><br><br> Earth Science.
OLga [1]

Answer:

-Growth of plants on the rock.

-Temperature and pressure changes in nature.

-Freezing and thawing of water in cracks of the rock.

-Formation of salt crystals within the rock.

-Burrowing by animals.

those are some factors I know

hope this helped you

4 0
3 years ago
Read 2 more answers
Difference between radical and compound
Elodia [21]

Answer:

A radical is an atom, ion, or molecule that has unpaired electrons.

A compound is a combination of two or more elements.

Explanation:

6 0
4 years ago
Which statements describes why ethyl methyl ether (b.p. 7.9°C) and 1-propanol (b.p. 97.2°C) have such different boiling points d
Lelu [443]

Answer:

B) 1-propanol has more hydrogen bonding than ethyl methyl ether.

Explanation:

1-propanol and ethyl methyl ether look very similar but have very different boiling points. They both have three carbon atoms but ethyl methyl ether has an oxygen atom.

Ethyl methyl ether has both London dispersion forces and dipole-dipole interactions.

1-Propanol has London dispersion forces, dipole-dipole interactions and hydrogen bonding.

1-propanol has more hydrogen bonding than ethyl methyl ether which explains why they both have different boiling points.

3 0
3 years ago
Cis-4-tertButylcyclohexyl bromide (compound 1) and Trans-4 tert Butylcyclohexylbromide (compound 2) are reacted with Potassium T
Mkey [24]

Answer:

In compound 1 the Tert butyl group occupies the equatorial position and the Bromine occupies the axial position and in compound 2 the Tert butyl occupies the axial and the bromine occupies equatorial positions. Compound 1 reacts faster than compound 2.

Explanation:

In cyclic organic compounds, substituents may occupy the axial or equatorial positions. The axial positions are aligned parallel to the symmetry axis of the ring while the equatorial positions are around the plane of the ring.

Bulky substituents have more room in the equatorial than in the axial position. This means that compound 1 is more stable than compound 2.

This is clear on the basis of stability of the molecules because compound 1 will react faster than compound 2 since the bulky tertiary butyl group in compound 1 occupy equatorial and not axial positions.

4 0
3 years ago
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