Answer:
34 g/100 mL
Explanation:
The solubility of a compound can be expressed in g/100mL, for this we must divide the mass of the compound that dissolves in the solute by the volume of the solvent.
The solvent, in this case, is water, and that mass of the solute X that dissolved is the mass that was recovered after the solvent was drained and evaporated. So the solubility of X (S) is:
S = 0.17 kg/5L
S = 170g/5000mL
S = 170g/(5*1000)mL
S = 34 g/100 mL
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Answer</h2>
2.626984127 m
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Explanation:</h2><h2>
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You have to know the equation that relates wavelength, frequency, and velocity (it's like speed but a bit different).
v = f x λ
where:
v = velocity
f = frequency
λ = Wavelength
Rearrange to make λ subject:
λ = v / f
We've been given 331 as the speed, 126 as the frequency. Sub it into the equation:
331 / 126 = 2.626984127 m
Answer:
The correct answer is:
An electron will be emitted in the second experiment, but it cannot be determined whether it will reach the second plate.
Explanation:
In fact, violet has higher frequency than green light. This means that photons on violet carry more energy than photons of green light (remember that the energy of a photon is proportional to it's frequency:

, so when they hit the surface of the metal, more energy is transferred to the electrons. The electron was already emitted with green light, so it must be emitted with also violet light, given the more energy transferred.
A homogeneous mixture has the same uniform appearance and composition throughout. Many homogeneous mixtures are commonly referred to as solutions. A heterogeneous mixture consists of visibly different substances or phases. The three phases or states of matter are gas, liquid, and solid.
Hope this helps you!
Complete Question:
check the first image for complete part of the question
Answer and Explanation:
Epoxide is a three membered ring made up of two carbon atoms and one oxygen atom. Epoxides are cyclic ethers. Due to its ring size, it is highly strained and very reactive. Epoxide ring opening takes place with respect to addition of acid and base.
Ring opening of epoxide with acid:
In the presence of base, the nucleophile attacks the epoxide ring at more substituted site and inverse stereochemistry takes place.(check file 2 attached)
Ring opening of epoxide with base:
The backside attack of nucleophile takes place in less substituted site and then it undergoes protonation to form a product.
(check file 2 attached)