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Answer:
Repeated SN2 reactions occur leading to the formation of a racemic mixture
Explanation:
S-2-iodooctane is a chiral alkyl halide with an asymmetric carbon atom. The presence of an asymmetric carbon atom implies that it can rotate plane polarized light and thus lead to optical isomerism. The two configurations of the compound are R/S according to the Cahn-Prelong-Ingold system.
However, when S-2-iodooctane is treated with sodium iodide in acetone, repeated SN2 reactions occur since the iodide ion is both a good nucleophile and a good leaving group. Hence a racemic modification is formed in the system with time hence we end up with (±)- Iodooctane.
When a specific amount of energy is emitted when excited electrons in an atom in a sample of an element return to the ground state, this emitted energy can
<span>be used to determine the "identity of the element".</span>
Answer;
it combines with the water and H in the atmosphere and creates sulfuric acid thus making the rain acidic
Explanation:
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.
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