Answer: 5 → 2
Explanation: An electron when given enough energy will get excited to the higher states and when it returns to the ground state will emit energy in the from of light.
The most energetic energy level will be 5 → 2 because in this, energy level 2 is the ground state and energy level 5 is the excited state . Thus more energy will be needed by the electron to move towards the higher excited state.
The energy required by the 4 → 2 energy level will be of medium level and
3 → 2 will require the least energy.
The image for the reference is shown below.
Answer:
The correct answer is 378 g of water
Explanation:
A concentration of 5.50% by mass means that there are 5.50 grams of solute in 100 grams of solution:
5.50 %m/m = 5.50 g solute/100 g solution
If we have 22.0 g of solute (KCl), we found the total mass of solution as follows:
5.50 g KCl ----- 100 g solution
22.0 g KCl ------ X = 22.0 g KCl x 100 g solution/ 5.50 g KCl = 400 g solution
22.0 g KCl/400 g solution = 5.5 g KCl/100 g solution = 5.50 % m/m
This is the total mass of solution (400 g). The mass of water we have to add is the following:
Mass water = 400.0 g solution - 22.0 g KCl = 378.0 g
So, in order to prepare a 5.50% m/m of solution, we have to weight 22.0 g of KCl and to add 378.0 g of water until reaching 400.0 g of total mass solution.
There are 6 Carbon atoms and 14 Hydrogen which makes it a Hexane
Answer:
The Earth's magnetic field intensity is roughly between 25,000 - 65,000 north magnetic pole is 86.50°N and 164.04°E and the south magnetic pole is 64.07°S and 135.88°E
Answer:
This is an example of
(substitution nucleophilic bimolecular) reaction
Explanation:
Conversion of t-butyl alcohol to t-butyl bromide proceeds through
(substitution nucleophilic bimolecular)mechanism.
In the first step, -OH group in t-butyl alcohol gets protonated.
In the second step, stable tertiary carbocation (t-butyl cation) is produced by removal of
.
In the third step, bromide ion attacks to t-butyl cation and produces t-butyl bromide.
Removal of
from n-butyl alcohol will produce an unstable primary carbocation (n-butyl cation). Hence, to produce this unstable carboction, large amount of activation energy is required. Therefore, n-butyl alcohol gives much slower reaction with HBr.
Reaction mechanism has been shown below.