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:
Its (d) hydrogen
Explanation:
just took the test on edg2020
Answer:
8) 45 volt
9) 8 ohms
100 volt
Explanation:
using ohms law all through
8) v = 3×15
9) R= 120/15
the last V=100×1
Answer:
a. Concave down
Linear increasing
b. Increases the reaction rate
c. The reaction approaches the saturation point of the enzyme
Explanation:
a. For the reaction with enzyme, the shape is concave down. The action of the enzyme on the preferred substrate is initially very rapid and decreases as the enzyme becomes saturated and the ratio of products to substrate increases to approach an equilibrium rate of reaction
For the reaction without enzyme, the shape is linear and increasing. Increase in the concentration of the substrate will increase the number of effective collisions that lead into product formation leading to an increased rate of the chemical reaction
b. The enzyme increases the proportion of effective combination of substrates to form the products
c. The curve of the reaction with enzyme flattens out because as the concentration of the substrate increases while that of the enzyme remains the same, the enzyme becomes saturated and less able to increase the rate of the reaction of the excess substrate.
