I believe the answer is 80. I am not sure
Answer:

Explanation:
Hello!
In this case, according to the reaction:

We can see there is a 4:2 mole ratio between chromium and chromium (III) oxide, this, for the given 56.2 g of chromium, the theoretical yield of the oxide product is computed down below:

Now, considering the 76.0-% yield for this reaction, the actual yield turns out:

Best regards!
Answer: 1-Phenyl ethyl radical is formed as an intermediate in the reaction and since Phenyl ethyl radical has a trigonal planar geometry so it is a planar molecule having two faces. So Br radical radical can recombine with the two faces with equal probability leading to a racemic mixture in 50:50ratio of products.Hence two products are formed which are known as enatiomers.
Explanation:
When we irradiate the ethylbenzene with UV light , it leads to homolytic cleavage and 1- Phenyl ethyl free radical is generated.
Phenyl ethyl free radical is generated because it is very stable as it is on a secondary carbon center as well as on a benzylic position so it can be stabilized by the resonance as well as inductive effect at the secondary carbon center.
NBS(N-bromosuccinimide) is a source of bromine radical and provides bromine free radical.
Once the 1- Phenyl ethyl free radical is generated then bromine free radical can recombine with benzyl free radical leading to product formation.
Since 1- Phenyl ethyl free radical has a trigonal planar geometry so it is a planar molecule which has two faces and hence the radical recombination with bromine free radical can occur with either of the two faces available.
Kindly refer the attachments for structure as well as the mechanism of the reaction.
So two isomers which are enantiomers are produced are obtained.
Answer:
Acceleration = 3.5 m.s⁻²
Explanation:
Definition:
The acceleration is rate of change of velocity of an object with respect to time.
Formula:
a = Δv/Δt
a = acceleration
Δv = change in velocity
Δt = change in time
Units:
The unit of acceleration is m.s⁻².
Acceleration can also be determine through following formula,
F = m × a
a = F/m
Given data:
Force = 35 N (N = Kg. m.s⁻²)
Mass = 10.0 Kg
a = ?
Formula:
a = F/m
a = 35 Kg. m.s⁻²/ 10.0 Kg
a = 3.5 m.s⁻²