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: The net ionic equation will be as follows.
Explanation:
The chemical equation for the given reaction is as follows.
We know that a strong acid or base will dissociate completely into a solvent whereas a weak acid or base dissociates partially into the solvent. Hence, the ionic equation will be as follows.
Now, we will cancel the spectator ions from the above equation. Therefore, the net ionic equation will be as follows.
or,
1) H2O is able to dissolve both polar molecules and non polar ones
2) due to its extreme polarity it can even dissolve some I onic compounds
3 the h2o molecule itself is small in size
Answer:
589.038 m/s
Explanation:
i dont know if did this right tho
Melamine should be the right answer, i hope this helps.