Quantum numbers describe values of conserved quantities in the dynamics of a quantum system. In the case of electrons, the quantum numbers can be defined as "the sets of numerical values which give acceptable solutions to the Schrödinger wave equation for the hydrogen atom
Answer 1:
Isomers are compounds with same molecular formula but different structure formula. Isomers are classified into two types
a) Structural/configurational isomers
b) Stereo isomers
In structural/configurational isomers atom and functional groups are attached in different fashion. Structural isomers may have different functional groups. Structural isomers are further classified as chain isomers, position isomers and functional isomers. In case of stereo-isomers, compounds have same functional group, but different orientation in space. They also have difference activity towards polarized light.
Answer 2:
Hexane has a molecular formula of C6H14. It exhibits following structural isomers
a) hexane<span>,
b) 2-methylpentane
c)3-methylpentane
d) 2,2-dimethylbutane
e) 2,3-dimethylbutane
Thus, in all there are 5 isomers of hexane
Answer 3:
</span><span>Butane has two possible isomers but that decane has 75 possible isomers. This can be attributed to the fact that butane has 4 carbon atoms, while decane has 10 carbon atom. As the number of carbon atom increases, there are higher possible sites of linkage, in different fashion. Therefore, as number 69 of carbon atoms increases, number of different possible isomers increases.
Answer 4:
It has been observed that, though isomers have same molecular formula, but the have different boiling points. Infact, branched isomers have lower boiling point as compared to linear isomers. For example, hexane has boiling point = 69 oC, 2 methyl pentane has boiling point = 60 oC, 2,4, dimethyl butane has boiling point = 58 oC and 2,2 dimethyl butane has boiling point = 50 oC. Thus, it can be observed that branched isomers have lower boiling points as compared to linear isomers. This can be attributed to lower van der Waal's forces of interaction in branched isomers as compared to linear isomers.
</span><span>
</span>
<h2><u>Answer</u> :</h2>
The most appropriate option is :

Since, they are the most abundant elements found in Earth's Crust.

The organic product formed when 1−hexyne is treated with H₂O, H₂SO₄, and HgSO₄ will be 2-hexanone (structure attached).
This reaction is an example of an oxymercuration reaction of the organic product 1−hexyne.
Oxymercuration is shown in three steps to the right. The nucleophilic double bond attacks the mercury ion, releasing an acetoxy group. The mercury ion's electron pair attacks carbon on the double bond, generating a positive-charged mercuronium ion. Mercury's dxz and 6s orbitals give electrons to the double bond's lowest unoccupied molecular orbitals.
In the second stage, the nucleophilic H₂O attacks the highly modified carbon, freeing its mercury-bonding electrons. Electrons neutralize mercury ions by collapsing. Water molecules have positive-charged oxygen.
In the third stage, the negatively charged acetoxy ion released in the first step attacks the hydrogen of the water group, generating the waste product HOAc. The two electrons in the oxygen-hydrogen link collapse into oxygen, neutralizing its charge and forming alcohol.
You can also learn about organic products from the following question:
brainly.com/question/13513481
#SPJ4