Energy levels inside an atom are the specific energies that electrons can have when energy occupies specific orbitals. Electrons can be excited to higher energy levels by absorbing energy from the surroundings, an equivalent light is emitted when an electron returns from a high energy state to a lower one. Representation of this diagrammatic is known as the energy level diagram.
Answer:
Okay the Answers are top to bottom.
5, 4, 1, 3, 2
Explanation:
Answer:
8.625 grams of a 150 g sample of Thorium-234 would be left after 120.5 days
Explanation:
The nuclear half life represents the time taken for the initial amount of sample to reduce into half of its mass.
We have given that the half life of thorium-234 is 24.1 days. Then it takes 24.1 days for a Thorium-234 sample to reduced to half of its initial amount.
Initial amount of Thorium-234 available as per the question is 150 grams
So now we start with 150 grams of Thorium-234
So after 120.5 days the amount of sample that remains is 8.625g
In simpler way , we can use the below formula to find the sample left
Where
is the initial sample amount
n = the number of half-lives that pass in a given period of time.
Answer:
The total weight of both object is 78.56 kg.
Explanation:
Given data:
Mass of object A = 45.1 kg
Mass of object B = 33.46 kg
Total weight of object = ?
Solution:
Total weight of both subject must be the sum of weight of object A and B.
Total weight of objects = weight of object A + weight of object B
Now we will put the values of mass of object A and B.
Total weight of objects = 45.1 kg + 33.46 kg
Total weight of objects =78.56 kg
Thus the total weight of both object is 78.56 kg.
Answer:
Nitrobenzene is too deactivated (by the nitro group) to undergo a Friedel-Crafts alkylation.
Explanation:
The benzene ring in itself does not easily undergo electrophilic substitution reaction. Some groups activate or deactivate the benzene ring towards electrophilic substitution reactions.
-NO2 ia a highly deactivating substituent therefore, Friedel-Crafts alkylation of nitrobenzene does not take place under any conditions.
This reaction scheme is therefore flawed because Nitrobenzene is too deactivated (by the nitro group) to undergo a Friedel-Crafts alkylation.
