the 2nd one is correct
The option that would most likely increase the rate for a more contentrated potassium hydrogene
:) hope this helps
Explanation:
Part a
Pyridine is an aromatic heterocyclic compound and undergoes nucleophilic aromatic substitution reaction at 2 and 4 positions.
This is because, when a nucleophile attack pyridine at 2 and 4 positions, the anoin formed is stabilized. In the anion formed is tabilized by resonance and also negative charge is present at electronegative atom, nitrogen.
If the nucleophile attack at 3 position, the anion formed is not as stable as anions formed when nucleophile attach at 2 and 4 positions. This is because negative charge is not present at the nitrogen atom.
Part b:
Tautomers are structural isomers of each others formed by migration atom within the molecule. Tautomers exist in equilibrium with each other.
Tautomers of 2-Hydroxypyridine and 4-Hydroxypyrine are given in the attachment.
Answer:
D
Explanation:
because the rest don’t make any sense
Answer: A reversible reaction is a reaction that takes place in back and front directions. If the reaction were to reach equilibrium, the rate of forward direction would be equal to that of the reverse reaction.
Explanation:
Reversible reactions :
These are the reaction in which reactants reacts to give product and products reacts to give reactants as a product in return.
- In above equation, 'A' and 'B' are reacting together to give 'C' and 'D', as products and vice-versa.
- When the above reaction reaches equilibrium the rate of forward and backward reaction becomes equal.