Since the question is incomplete, the table has been searched in order to comply with the question.
Based on the table that I have provided, the order of increasing
depth from shallowest to deepest are the following; A,B,C,D,E. The reason that
this is the order to be chosen because the one responsible for making water
dense is the salt that is on the water and by that, the base is likely to sink
whereas the ones with less salt won’t be as thick compared those who have much
salt and will skim on its top.
The Oxyfuel gas or flame refers to a group of welding processes that use the flame produced by the combination of a fuel gas and oxygen as the source of heat.
<u>Explanation:</u>
- Oxy-fuel welding is a process that utilizes fuel gases and oxygen to weld metals. Oxyfuel gas or flame refers to a group of welding processes that utilize the flame delivered by the blending of fuel gas and oxygen as the source of heat.
- This flame is utilized for cutting and welding of two metallic pieces. This is done due to the heat produced by cutting and welding of two metallic pieces together by heating to the melting point.
- An oxyhydrogen flame is utilized for cutting and welding of two metallic pieces due to the heat produced by the flame, i.e, 2800 ° C. At this temperature, the metal gets softened effectively and thus it can easily separate or welded together.
Remember that a conjugate acid-base pair will differ only by one proton.
None of the options you listed are conjugate acid-base pairs as none of them differ only by one proton (or H⁺)
An example of a conjugate acid-base pair would be NH₃ and NH₄⁺NH₃ + H₂O --> NH₄⁺ + OH⁻NH3 is the base, and NH₄⁺ is the conjugate acid
Answer:
mendeleev left a space
Explanation:
so the periodic table can be organize
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.