Answer:
See the image 1
Explanation:
If you look carefully at the progress of the SN2 reaction, you will realize something very important about the outcome. The nucleophile, being an electron-rich species, must attack the electrophilic carbon from the back side relative to the location of the leaving group. Approach from the front side simply doesn't work: the leaving group - which is also an electron-rich group - blocks the way. (see image 2)
The result of this backside attack is that the stereochemical configuration at the central carbon inverts as the reaction proceeds. In a sense, the molecule is turned inside out. At the transition state, the electrophilic carbon and the three 'R' substituents all lie on the same plane. (see image 3)
What this means is that SN2 reactions whether enzyme catalyzed or not, are inherently stereoselective: when the substitution takes place at a stereocenter, we can confidently predict the stereochemical configuration of the product.
Simple 6L of air times the .21L of O2 = 1.26
Generally when we move down the group on a periodic table the atomic radii increases as the valency electrons occupy higher levels due to the increasing quantum number. Hence the atomic radii increases down the group.
The ionic radii increases down the group because while we move down the group the elements gain electrons and form ions called anions as an additional electron occupies the orbital the ions get bigger in size. Hence the ionic radii increase.
Electronegativity is described as the ability to attract and bind with electrons and it is a qualitative property. It decreases as we move down the group because the distance between the valency electrons and the nucleus increases. Hence electronegativity decreases down the group.
Reactivity increases as we move down the group as the metals have the tendency to lose electron form its outer shell.
Therefore the answer is ionic radii increases.
Answer:
cant understand the grammer rewrite and ill answer
Explanation:
