Answer: a. 6(3x2=6)
B. 4(4x1=4)
C. 6(4(1)+2(1)=4+2=6
D. 4
E. 6(3(2)=6)
F. 4(2(1)+2(1)[2+2=4)
G. 5(5(1)=5)
H. 4(2(1)+2(1)=2+2=4)
Explanation:
Coordination number= no of ligands
= No of ligands X denticity
Denticity is nothing but type of ligands like mono,do and tetradentate ligands.
Answer:
rate = [NO]²[H₂]
Explanation:
2NO + H2 ⟶N2 + H2O2 (slow)
H2O2 + H2 ⟶2H2O (fast)
From the question, we are given two equations.
In chemical kinetics; that is the study of rate reactions and changes in concentration. The rate law is obtained from the slowest reaction.
This means that our focus would be on the slow reaction. Generally the rate law is obtained from the concentrations of reactants in a reaction.
This means our rate law is;
rate = [NO]²[H₂]
Answer:
Nuclear transmutation
Explanation:
The process in which an element spontaneously transforms into another isotope of the same element, or into a different element is called nuclear transumutation. It occurs when the number of protons or neutrons in the nucleus of an atom is changed.
Answer:
A. Methanol
B. 2-chloropropan-1-ol
C. 2,2-dichloroethanol
D. 2,2-difluoropropan-1-ol
Explanation:
Primary alcohols are stronger acids than secondary alcohols which are stronger than tertiary alcohols.
This trend is so because of the stability of the alkoxide ion formed(stabilising the base, increases the acidity). A more stabilised alkoxide ion is a weaker conjugate base (dissociation of an acid in water).
By electronic factors, When there are alkyl groups donating electrons, the density of electrons on th O- will increase a d thereby make it less stable.
By stearic factors, More alkyl group bonded to the -OH would mean the bulkier the alkoxide ion which would be harder to stabilise.
Down the group of the periodic table, basicity (metallic character) decreases as we go from F– to Cl– to Br– to I– because that negative charge is being spread out over a larger volume that is electronegativity decreases down the group.
Electronegative atoms give rise to inductive effect and a decrease in indutive effects leads to a decrease in acidity. Therefore an Increasing distance from the -OH group lsads to a decrease in acidity.
From above,
A. Methanol
B. 2-chloropropan-1-ol
C. 2,2-dichloroethanol
D. 2,2-difluoropropan-1-ol
