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Harlamova29_29 [7]
4 years ago
9

Which acid is the best choice to create a buffer with ph= 3.19?

Chemistry
1 answer:
Crazy boy [7]4 years ago
5 0
<span>The best choice is hypochlorous acid nitrous acid (HNO2) because it has the nearest value of pK to the desired pH.
pKa of </span>nitrous acid<span> is 3.34 
If we know pKa and pH values,  we can calculate the required ratio of conjugate base (NO2⁻) to acid (HNO2) from the following equation:
pH=pKa + log(conc. of base)/( conc. of acid)
</span><span>3.19=3.34 + log c(NO2⁻)/c(HNO2)
</span><span>3.19 - 3.34 = log c(NO2⁻)/c(HNO2)
-0.15 = log c(NO2⁻)/c(HNO2)
c(NO2⁻)/c(HNO2) = 10⁰¹⁵ = 1.41

</span>
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Does taking away an electron change the position on the periodic table?
mafiozo [28]

Answer:

Basically no it doesnt it stays the same it just means your adding more onto the atomic number and it keeps position

As the atomic number increases along a row of the periodic table, additional electrons are added to the same, outermost shell. The radius of this shell gradually contracts as the attraction between the additional electrons and the nucleus increases.

Explanation:

7 0
3 years ago
Do anyone know how to do question B
Over [174]

Answer:

a) IUPAC Names:

                   1) (<em>trans</em>)-but-2-ene

                   2) (<em>cis</em>)-but-2-ene

                   3) but-1-ene

b) Balance Equation:

                       C₄H₁₀O + H₃PO₄   →   C₄H₈ + H₂O + H₃PO₄

As H₃PO₄ is catalyst and remains unchanged so we can also write as,

                                    C₄H₁₀O   →   C₄H₈ + H₂O

c) Rule:

           When more than one alkene products are possible then the one thermodynamically stable is favored. Thermodynamically more substituted alkenes are stable. Furthermore, trans alkenes are more stable than cis alkenes. Hence, in our case the major product is trans alkene followed by cis. The minor alkene is the 1-butene as it is less substituted.

d) C is not Geometrical Isomer:

        For any alkene to demonstrate geometrical isomerism it is important that there must be two different geminal substituents attached to both carbon atoms. In 1-butene one carbon has same geminal substituents (i.e H atoms). Hence, it can not give geometrical isomers.

7 0
3 years ago
Carbon-14 has a half-life of 5730 years. In a plant fossil, you find that the 14C has decayed to 1/8.00 of the original amount.
Crank
Take three half lives.

5730 x 3 = 17190
5 0
4 years ago
Draw the product formed when the following diene is treated with one equivalent of HCl. Do not show stereochemistry in your answ
garri49 [273]

Answer:

4-chloro-4-methyl-cyclohexene.

Explanation:

Hello,

On the attached picture you will find the chemical reaction forming the required product, 4-chloro-4-methyl-cyclohexene. In this case, according to the Markovnicov’s rule, it is more likely for the chlorine to be substituted at the carbon containing the methyl radical in addition to the hydrogen to the next carbon to break the double bond and yield the presented product.

Best regards.

6 0
3 years ago
in a titration a 25.0 ml of 0.500 m khp is titrated to the equivalence point NaOH. The final solution volume is 35.5 mL. what is
borishaifa [10]
M2= 0.35M

Formula: M1 • V1 = M2 • V2

1) 25.0mL • .500M = 35.5mL • (x)

2) 12.5 = 35.5 • (x)

3) 12.5/35.5 = x

4) 0.35211 = x = M2

Hope this helps!
5 0
3 years ago
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