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:
Nervous system messages travel through neurons as electrical signals. When these signals reach the end of a neuron, they stimulate the release of chemicals called neurotransmitters. Neurotransmitters travel across synapses, spaces between neurons or between neurons and other body tissues and cells.
Explanation:
Answer:
The formula of Organic acid is as follow,
R-COOH
Explanation:
The class of organic acids is called Carboxylic Acids. In above general structure, R is alkyl group and can vary. While -COOH is the functional group.
Carboxylic Acids has the tendency to loose protons and their pKa value depends upon the alkyl group. For example the pKa value of Acetic acid (R = -CH₃) is 4.7. The driving force for this acidity is the stability of carboxylate (conjugate base) due resonance. i.e
RCOOH ⇄ RCOO⁻ + H⁺
Where;
RCOO⁻ = Carboxylate Ion (Conjugate base)
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Answer:
theory
Explanation:
Fits all criteria
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