A because I said so I know so
Answer:
<em>lithosphere</em><em> </em><em>(land)</em>
<em>hydrosphere (water)</em>
<em>biosphere</em><em> </em><em>(living things)</em>
<em>atmosphere (air).</em>
Answer:
In an electrophilic aromatic substitution (Friedel Crafts alkylation) first in the monoalkylation of the 1,4-dimethoxybenzenethe the methoxy groups redirects the substitution for ortho-para positions with respect to the electrophile that is going to enter (alkyl group) this is due to the increase in electron density in that position, that is , to the inductive effect.
According to the second incoming alkyl group there would be 3 positions available, from which it will choose the meta position in relation to the second methoxy group, since the alkyl group is a weak activator of the ortho meta positions and coincides with the position to which it redirects the second methoxy group.
The 2s orbital different than the 1s orbital because the 2s orbital extends farther from the nucleus than the 1s.
As we move away from the nucleus, the values of the principal quantum number (n) continues to increase.
As the principal quantum number (n) increases, the orbital becomes farther away from the nucleus.
The higher energy orbital are always larger than the orbitals closer to the nucleus.
Hence, the 2s orbital different than the 1s orbital because the 2s orbital extends farther from the nucleus than the 1s.
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