Answer:
-290KJ/mol
Explanation:
ΔHrxn = ΔHproduct - ΔHreactant
ΔHrxn= 4ΔHH3PO4 - {6ΔHH2O + ΔHP4O10}
ΔHrxn = 4(-1279) - [6(-286) - 3110]
= -5116 -(-1716-3110)
= -5116-(-4826)
= -5116 + 4826 = -290KJ/mol
C
Why? As you increased energy levels the distance between two energy levels gets larger. This is often due to shielding
Answer:
1.3 × 10³ cm³
Explanation:
The gas occupies a volume of V₁ = 310 cm³ under standard temperature and pressure (STP), that is, T₁ = 273.15 K and P₁ = 1.0 atm. In order to find the volume V₂ under different conditions we can use the combined gas law formula.

Answer:
covalent
Explanation:
The carbon and the nitrogen very often form bonds in nature, carbon-nitrogen bonds, which are covalent types of bonds. In fact, the bonds between the carbon and nitrogen are one of the most abundant in the biochemistry and the organic chemistry. The bonds between these two can be double bonds, as well as triple bonds. The carbon-nitrogen bonds have the tendency to be strongly polarized toward the nitrogen.
The question is incomplete. Complete question is attached below
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Correct Answer:
Option C i.e. I ~ III < IV < V < II
Reason:
During a nucleophilic subsitution reaction of chloroarenes, Cl- group is replaced by an nucleophile like OH-.
Order of reactivity, during such reactions depends on the electron density on carbon atom that is attached to Cl. Lower the electron density, greater will be the reactivity.Among the provided chloroarenes, electron density on C atom will be minimum in case of compound II, because of presence of electron withdrawing group (-NO2) at ortho and para position. Due to this, there will be large number of resonating structures. This signifies greater electron de-localization, and hence largest reactivity for nucleophilic substitution reaction.
Followed by this, compound V will show greater reactivity, due to presence of -NO2 group at para and one of the ortho position. Compound IV will have less number of resonating structures as compared to compound II and V, hence it will display poor reactivity towards nucleophilic substitution reaction.
Finally, compound 1 and III will minimum reactivity towards nucleophilic substitution reaction, because -NO2 group present at meta position (compound III) will not participate in resonance.