It’s
1.A
2.C
3.B
hope it’s correct
I believe the answer is C
Answer: option <span>A) increases from bottom to top within the group.
Explanation:
</span>It is a known trend that the metallic character of the elements increase from let to right and from top to bottom.
The greater the metallic character the greater the reactivity of the metal.
So, the elements of the columns 1 and 2 are the most reactive metals and among them the elements at the bottom are yet more reactive.
<span>The higher reactivity of the metals that are lower in the periodic table is attributed to the greater total number of electrons.
The greater the total number of electrons the more reactive the metals
as their outermost electrons (the valence electrons which are those that react) are located further from the nucleus and therefore they are held less
strongly, which makes them react more easily.</span>
Answer:The product formed on reaction with hydroxide ion as nucleophile is 2R-hexane-2-ol.
The product formed on reaction with water would be a 50:50 mixture of
2S-hexane-2-ol. and 2R-hexane-2-ol.
Explanation:
2S-iodohexane on reactiong with hydroxide ion would undergo SN² substitution reaction that is substitution bimolecular. Hydroxide ion has a negative charge and hence it is a quite good nucleophile .
The rate of a SN² reaction depends on both the substrate and nucleophile . Here the substrate is a secondary carbon center having Iodine as a leaving group.SN² reaction takes place here as hydroxide ion is a good nucleophile and it can attack the secondary carbon center from the back side leading to the formation of 2R-hexane-2-ol.
In a SN² reaction since the the nucleophile attacks from the back-side so the product formation takes place with the inversion of configuration.
When the same substrate S-2-iodohexane undergoes a substitution reaction with water as a nucleophile then the reaction occurs through (SN¹) substitution nucleophilic unimolecular mechanism .
The rate of a SN¹ reaction depends only on the nature of substrate and is independent of the nature of nucleophile.
The SN¹ reaction is a 2 step reaction , in the first step leaving group leaves leading to the formation of a carbocation and once the carbocation is formed then any weaker nucleophile or even solvent molecules can attack leading the formation of products.
In this case a secondary carbocation would be generated in the first step and then water will attack this carbocation to form the product in the second step.
The product formed on using water as a nucleophile would be a racemic mixture of R and S isomers of hexane -2-ol in 50:50 ratio. The two products formed would be 2R-hexane-2-ol and 2S-hexane-2-ol.
Kindly refer the attachment for reaction mechanism and structure of products.
Explanation:
The solubility curve helps us to compare the solubility of difference substances at same temperature. It gives the idea that solubility changes with the temperature. The solubility curve helps us to predict which substance will crystalize out first from hot solution containing two or more solutes.