Answer:
Part (i)
Z = 39.06 ohm
Part (ii)
R = 21.7 ohm
Explanation:
a) here we know that
maximum value of EMF = 125 V
maximum value of current = 3.20 A
now by ohm's law we can find the impedence as
now we will have
Part b)
Now we also know that
now we have
Answer:
The ball would have landed 3.31m farther if the downward angle were 6.0° instead.
Explanation:
In order to solve this problem we must first start by doing a drawing that will represent the situation. (See picture attached).
We can see in the picture that the least the angle the farther the ball will go. So we need to find the A and B position to determine how farther the second shot would go. Let's start with point A.
So, first we need to determine the components of the velocity of the ball, like this:
we pick the positive one, so it takes 0.317s for the ball to hit on point A.
so now we can find the distance from the net to point A with this time. We can find it like this:
Once we found the distance between the net and point A, we can similarly find the distance between the net and point B:
t= -0.9159s or t=0.468s
we pick the positive one, so it takes 0.468s for the ball to hit on point B.
so now we can find the distance from the net to point B with this time. We can find it like this:
So once we got the two distances we can now find the difference between them:
so the ball would have landed 3.31m farther if the downward angle were 6.0° instead.
It will travel slowest through gases.
Answer:
D
Explanation:
- The rate of the Diels-Alder is orders of magnitude faster if there is an electron-withdrawing group on the dienophile. For example, replacing a hydrogen on ethene with the electron-withdrawing group CN results in about a 10^5 increase in the reaction rate.
- Other common electron withdrawing functional groups that will accelerate the Diels Alder reaction of dienophiles include aldehydes, ketones, and esters.
- In short, any functional group conjugated with the pi bond which can act as a pi acceptor will accelerate a Diels-Alder reaction with a typical diene.
- See attachment for graphical explanation.