The energy of the photon from the calculation performed is 3.5 * 10^-16 J.
<h3>What is a photon?</h3>
A photon is a packet of light. It was derived from the theory of Albert Einstein. The energy of a photon is obtained from; E = hc/λ
- h= Plank's constant
- c = speed of light
- λ = wavelength
Now we have that;
E = 6.6 * 10^-34 * 3 * 10^8/562 * 10^-9
E = 3.5 * 10^-16 J
Missing parts:
Calculate the energy, in joules, of a photon of green light having a wavelength of 562nm?
Learn more about energy of photon:brainly.com/question/20912241
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Answer:
Percentage composition = 14.583%
Explanation:
In chemistry, the emprical formular of a compound is the simplest formular a compound can have. It shows the simplest ratio in which the elements are combined in the compound.
Percentage composition by mass of Nitrogen
Nitrogen = 14g/mol
In one mole of the compound;
Mass of Nitrogen = 1 mol * 14g/mol = 14g
Mass of compound = 1 mol * 96.0 g/mol = 96
Percentage composition of Nitrogen = (Mass of Nitrogen / Mass of compound) * 100
percentage composition = 14/96 * 100
Percentage composition = 0.14583 * 100
Percentage composition = 14.583%
A is Ea, which stands for activating energy. Energy is needed to get the reaction underway and Ea is the energy needed to “start” the reaction.
B is the temperature either released or absorbed.
The diagram shows that the reaction is exothermic based on the fact that the products energy is lower than the reactants. That is because energy (which is temperature in this case) is released during the process. If the reactants would have been lower than the products, the reaction would be endothermic.
Water is H2O but I'm not sure about solids.
Answer:
Here's what I get
Explanation:
You may have done a Williamson synthesis of guaifenesin by reacting guaiacol with 3-chloropropane-1,2-diol.
A. Mechanism
Step 1
NaOH converts guaiacol into a phenoxide ion.
Step 2
The phenoxide acts as the nucleophile in an SN2 reaction to displace the Cl from the alkyl halide.
B. Improve the yield
You probably carried out the reaction in ethanol solution — a polar protic solvent.
You might try doing the reaction in a polar aprotic solvent— perhaps DMSO.
A polar aprotic solvent does not hydrogen bond to nucleophiles, so they become stronger.
C. Another method of ether synthesis —dehydration of alcohols
Sulfuric acid catalyzes the conversion of primary alcohols to ethers.
This is also a nucleophilic displacement reaction.
Protonation of the OH converts it into a better leaving group.
Attack by a second molecule of alcohol forms the protonated ether.
A molecule of water then removes the proton.
