Answer:
Explanation:
19) it is 3d10 instead of 4d10
20) it is missing 3p6, and 4s2 before 3d5
21) Ra is not a noble gas
22) Cs is not a noble gas
Answer:
It depends on what kind and how much. Some are about $100, and others are $1,000.
We know that Weighted atomic mass of Element is Calculated based upon their existence of isotopes and the Relative abundance of these isotopes.
Given that the Element X is Composed of :
Isotope Relative abundance Atomic Mass
⁵⁵X 70% 55
⁵⁶X 20% 56
⁵⁷X 10% 57
Weighted Atomic Mass of Element X :
= (0.70)(55) + (0.20)(56) + (0.10)(57)
= 38.50 + 11.2 + 5.70
= 55.4
So, the Weighted Atomic Mass of Element X is 55.4
not sure but h = hydrogen and o = oxygen
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.