Answer:
Silicon atoms have 14 protons.
Silicon atoms will react with other atoms in order to gain stability.
Silicon atoms have 14 electrons.
- E(Bonds broken) = 1371 kJ/mol reaction
- E(Bonds formed) = 1852 kJ/mol reaction
- ΔH = -481 kJ/mol.
- The reaction is exothermic.
<h3>Explanation</h3>
2 H-H + O=O → 2 H-O-H
There are two moles of H-H bonds and one mole of O=O bonds in one mole of reactants. All of them will break in the reaction. That will absorb
- E(Bonds broken) = 2 × 436 + 499 = 1371 kJ/mol reaction.
- ΔH(Breaking bonds) = +1371 kJ/mol
Each mole of the reaction will form two moles of water molecules. Each mole of H₂O molecules have two moles O-H bonds. Two moles of the molecule will have four moles of O-H bonds. Forming all those bond will release
- E(Bonds formed) = 2 × 2 × 463 = 1852 kJ/mol reaction.
- ΔH(Forming bonds) = - 1852 kJ/mol
Heat of the reaction:
is negative. As a result, the reaction is exothermic.
Answer:
pH = 1.32
Explanation:
H₂M + KOH ------------------------ HM⁻ + H₂O + K⁺
This problem involves a weak diprotic acid which we can solve by realizing they amount to buffer solutions. In the first deprotonation if all the acid is not consumed we will have an equilibrium of a wak acid and its weak conjugate base. Lets see:
So first calculate the moles reacted and produced:
n H₂M = 0.864 g/mol x 1 mol/ 116.072 g = 0.074 mol H₂M
54 mL x 1L / 1000 mL x 0. 0.276 moles/L = 0.015 mol KOH
it is clear that the maleic acid will not be completely consumed, hence treat it as an equilibrium problem of a buffer solution.
moles H₂M left = 0.074 - 0.015 = 0.059
moles HM⁻ produced = 0.015
Using the Henderson - Hasselbach equation to solve for pH:
ph = pKₐ + log ( HM⁻/ HA) = 1.92 + log ( 0.015 / 0.059) = 1.325
Notes: In the HH equation we used the moles of the species since the volume is the same and they will cancel out in the quotient.
For polyprotic acids the second or third deprotonation contribution to the pH when there is still unreacted acid ( Maleic in this case) unreacted.
Answer:The functional groups in an organic compound can frequently be deduced from its infrared absorption spectrum. A compound, C5H10O2, exhibits strong, broad absorption across the 2500-3200 cm^1 region and an intense absorption at 1715 cm'^-1. Relative absorption intensity: (s)=strong, (m)-medium, (w) weak. What functional class(cs) docs the compound belong to List only classes for which evidence is given here. Attach no significance to evidence not cited explicitly. Do not over-interpret exact absorption band positions. None of your inferences should depend on small differences like 10 to 20 cm^1. The functional class(es) of thla compound is(are) alkane (List only if no other functional class applies.) alkene terminal alkyne internal alkyne arene alcohol ether amine aldehyde or ketone carboxylic acid ester nitr
Glucose is the simplest sugar and carbohydrate that provides energy. The simplified model of glucose (C₆H₁₂O₆) shows carbon, hydrogen, and oxygen atoms linked together.
<h3>What is glucose?</h3>
Glucose is an example of a carbohydrate macromolecule that is further classified as a monosaccharide. They are crystalline and fundamental units of carbohydrates.
The molecular formula of glucose is C₆H₁₂O₆ and the mass is 180.156 g/mol. It is an aldohexose that contains an aldehydic functional group. In its structure, there are six oxygen atoms, six carbon atoms, and twelve hydrogen atoms.
Therefore, the glucose molecule is composed of C, H, and O.
Learn more about glucose here:
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