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.
Answer:
Mechanism for top reaction is combustion while the side product at bottom path oximes
Explanation:
Hydroxiamine is a reducing agent that requires high temperature to combust in it'd ageous state to produced oxime while water is eliminated. The reverse is the case because the production of water during combustion I does not yield the fight result as it can e very irritating.
Increased temperature stimulates the protons to become free to combust and react with 2 butene and other aldehyde during chemical reaction.
In a crystal, the molecules are closer together as they are in any solid. they have less room to move, and might even be combined together rather than individual
Iodine 131 and iodine 126 are the same in the sense that, they both have the same number of electrons and protons in their atoms, it is only the number of their neutrons that is different. Iodine 131 has 78 neutrons while iodine 126 has 73 neutrons.