Explanation:
I think the notation used to represent beta is B
Answer:
41 g
Explanation:
We have a buffer formed by a weak acid (C₆H₅COOH) and its conjugate base (C₆H₅COO⁻ coming from NaC₆H₅COO). We can find the concentration of C₆H₅COO⁻ (and therefore of NaC₆H₅COO) using the Henderson-Hasselbach equation.
pH = pKa + log [C₆H₅COO⁻]/[C₆H₅COOH]
pH - pKa = log [C₆H₅COO⁻] - log [C₆H₅COOH]
log [C₆H₅COO⁻] = pH - pKa + log [C₆H₅COOH]
log [C₆H₅COO⁻] = 3.87 - (-log 6.5 × 10⁻⁵) + log 0.40
[C₆H₅COO⁻] = [NaC₆H₅COO] = 0.19 M
We can find the mass of NaC₆H₅COO using the following expression.
M = mass NaC₆H₅COO / molar mass NaC₆H₅COO × liters of solution
mass NaC₆H₅COO = M × molar mass NaC₆H₅COO × liters of solution
mass NaC₆H₅COO = 0.19 mol/L × 144.1032 g/mol × 1.5 L
mass NaC₆H₅COO = 41 g
Answer is: Ksp = 4s³.
Balanced chemical reaction (dissociation) of strontium hydroxide:
Sr(OH)₂(s) → Sr²⁺(aq) + 2OH⁻(aq).
Ksp(Sr(OH)₂) = [Sr²⁺]·[OH⁻]².<span>
[</span>Sr²⁺] = s.<span>
[</span>OH⁻] = [Sr²⁺] = 2s<span>
Ksp = (2s)² · x = 4s³.
Ksp is the solubility product constant for
a solid substance dissolving in an aqueous solution.
[</span>Sr²⁺]
is equilibrium concentration of iumcations.<span>
[</span>OH⁻] is equilibrium concentration of hydroxide anions.
The equation is already balanced.
Answer:
Explanation:
In this case we want to know the structures of A (C6H12), B (C6H13Br) and C (C6H14).
A and C reacts with two differents reagents and conditions, however both of them gives the same product.
Let's analyze each reaction.
First, C6H12 has the general formula of an alkene or cycloalkane. However, when we look at the reagents, which are HBr in ROOR, and the final product, we can see that this is an adition reaction where the H and Br were added to a molecule, therefore we can conclude that the initial reactant is an alkene. Now, what happens next? A is reacting with HBr. In general terms when we have an adition of a molecule to a reactant like HBr (Adding electrophyle and nucleophyle) this kind of reactions follows the markonikov's rule that states that the hydrogen will go to the carbon with more hydrogens, and the nucleophyle will go to the carbon with less hydrogen (Atom that can be stabilized with charge). But in this case, we have something else and is the use of the ROOR, this is a peroxide so, instead of follow the markonikov rule, it will do the opposite, the hydrogen to the more substituted carbon and the bromine to the carbon with more hydrogens. This is called the antimarkonikov rule. Picture attached show the possible structure for A. The alkene would have to be the 1-hexene.
Now in the second case we have C, reacting with bromine in light to give also B. C has the formula C6H14 which is the formula for an alkane and once again we are having an adition reaction. In this case, conditions are given to do an adition reaction in an alkane. bromine in presence of light promoves the adition of the bromine to the molecule of alkane. In this case it can go to the carbon with more hydrogen or less hydrogens, but it will prefer the carbon with more hydrogens. In this case would be the terminal hydrogens of the molecules. In this case, it will form product B again. the alkane here would be the hexane. See picture for structures.