Answer: the answer is B
Explanation: i go to connexus i had this question
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.
Answer:
a. 3-methylbutan-2-ol
b. 2-methylcyclohexan-1-ol
Explanation:
For this reaction, we must remember that the hydroboration is an <u>"anti-Markovnikov" reaction</u>. This means that the "OH" will be added at the <em>least substituted carbon of the double bond.</em>
In the case of <u>2-methyl-2-butene</u>, the double bond is between carbons 2 and 3. Carbon 2 has two bonds with two methyls and carbon 3 is attached to 1 carbon. Therefore <u>the "OH" will be added to carbon three</u> producing <u>3-methylbutan-2-ol</u>.
For 1-methylcyclohexene, the double bond is between carbons 1 and 2. Carbon 1 is attached to two carbons (carbons 6 and 7) and carbon 2 is attached to one carbon (carbon 3). Therefore<u> the "OH" will be added to carbon 2</u> producing <u>2-methylcyclohexan-1-ol</u>.
See figure 1
I hope it helps!