<h2>Answer:</h2>
It means the waves collides and constructive interference occurred.
<h3>Explanation:</h3>
If the two waves coming from the opposite direction collide with each other, there are two way of their interference.
- Constructive interference: An interference which results in the increase in energy. And it is when crust of a wave comes on the crust of second wave.
- Destructive interference: An interference which results in decrease in energy of the resulting wave and colliding waves cancel the result of each other.
Hence in experiment there will be constructive interference.
Answer:
An ionic compound is formed when there is a reaction between the elements whose ions are electrostatically attracted.
Explanation:
The ionic compounds form crystalline networks with ionic bonding. Electrostatic attraction is a very strong bond that is very difficult to break. The stability of the ionic compound depends on the lattice energy, the higher it is, the more stable the compound is and the lattice energy is that which is released in the formation. At room temperature they are always in a solid state, because the bonds are very close and as stated before, they are difficult to break (providing a lot of energy)
Answer:
Don't mark me brainliest because of this but I'm pretty sure your supposed to give us the words because teachers don't give you things like that without the words you will the answer in with.
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.