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.
Law of conservation of mass- The total mass after a chemical reaction is exactly the same as the mass before.
Answer:
true
Explanation:
when molecules of a solid substance is vibrating so, it means they are possessing average kinetic energy. thus, we can conclude that the statement all the molecules of a substance posses the average kinetic energy value is true.
Answer:
Due to the short term of its action it has in the stomach environment
Explanation:
Aluminum hydroxide, magnesium hydroxide, and simethicone is a combination drug used for the treatment of upset stomach, acid indigestion, bloating heartburn caused by gas, or stomach discomfort caused by eating or drinking too much