Answer:
1) HNO3/H2SO4, 2) CH3CH2CH2Cl/AlCl3
Explanation:
Benzene is a stable aromatic compound hence it undergoes substitution rather than addition reaction.
When benzene undergoes substitution reaction, the substituent introduced into the ring determines the position of the incoming electrophile.
If I want to synthesize m-nitropropylbenzene, I will first carry out the nitration of benzene using HNO3/H2SO4 since the -nitro group is a meta director. This is now followed by Friedel Craft's alkykation using CH3CH2CH2Cl/AlCl3.
If new evidence or observations falsify a scientific theory, the theory will have to be changed to adapt to the new data or just discarded altogether.
Correct Answer: Option C
Reason:
<span>The </span>Pauli Exclusion Principle<span> states as '<em>in an atom or molecule, no two electrons can have the same four electronic quantum numbers. Further, an orbital can contain a maximum of only two electrons, the two electrons must have opposing spins.</em>'
</span>
Thus, it can be seen that in option C, electrons in last 2 subshell have electrons with same spin, which is a violation of Pauli Exclusion Principle .
The second stage of photosynthesis also called Calvin stage produces glucose