The main constituent of gallstones is cholesterol. Cholesterol may have a role in heart attacks and blood clot formation. Its elemental percentage composition is 83.87% C, 11.99% H, and 4.14% O. It has a molecular weight of 386.64 amu. Empirical formula is C₃H₄O₁ and Molecular formula is 7(C₃H₄O₁).
<h3>What is Empirical Formula ?</h3>
Empirical formula is the simplest whole number ratio of atoms present in given compound.
Element % Atomic mass Relative no. of atoms Simplest whole ratio
C 83.87 12 
= 6.98 
= 3
H 11.99 1 
= 11.09 
= 4
O 4.14 16 
= 0.25 
= 1
Thus the empirical formula is C₃H₄O₁.
<h3>How to find the Molecular formula of compound ?</h3>
Molecular formula = Empirical formula × n
n = 
= 
= 7
Molecular formula = Empirical formula × n
= 7 (C₃H₄O₁)
Thus from the above conclusion we can say that The main constituent of gallstones is cholesterol. Cholesterol may have a role in heart attacks and blood clot formation. Its elemental percentage composition is 83.87% C, 11.99% H, and 4.14% O. It has a molecular weight of 386.64 amu. Empirical formula is C₃H₄O₁ and Molecular formula is 7(C₃H₄O₁).
Learn more about the Empirical Formula here: brainly.com/question/1603500
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Answer:
Explanation:
The HF is about five million times as strong as phenol, so it will be by far the major contributor of hydronium ions. We can ignore the contribution from the phenol.
1 .Calculate the hydronium ion concentration
We can use an ICE table to organize the calculations.
HF + H₂O ⇌ H₃O⁺ + F⁻
I/mol·L⁻¹: 2.7 0 0
C/mol·L⁻¹: -x +x +x
E/mol·L⁻¹: 2.7 - x x x
![K_{\text{a}} = \dfrac{\text{[H}_{3}\text{O}^{+}] \text{F}^{-}]} {\text{[HF]}} = 7.2 \times 10^{-4}\\\\\dfrac{x^{2}}{2.7 - x} = 7.2 \times 10^{-4}\\\\\text{Check for negligibility of }x\\\\\dfrac{2.7}{7.2 \times 10^{-4}} = 4000 > 400\\\\\therefore x \ll 2.7\\\dfrac{x^{2}}{2.7} = 7.2 \times 10^{-4}\\\\x^{2} = 2.7 \times 7.2 \times 10^{-4} = 1.94 \times 10^{-3}\\x = 0.0441\\\text{[H$_{3}$O$^{+}$]}= \text{x mol$\cdot$L$^{-1}$} = \text{0.0441 mol$\cdot$L$^{-1}$}](https://tex.z-dn.net/?f=K_%7B%5Ctext%7Ba%7D%7D%20%3D%20%5Cdfrac%7B%5Ctext%7B%5BH%7D_%7B3%7D%5Ctext%7BO%7D%5E%7B%2B%7D%5D%20%5Ctext%7BF%7D%5E%7B-%7D%5D%7D%20%7B%5Ctext%7B%5BHF%5D%7D%7D%20%3D%207.2%20%5Ctimes%2010%5E%7B-4%7D%5C%5C%5C%5C%5Cdfrac%7Bx%5E%7B2%7D%7D%7B2.7%20-%20x%7D%20%3D%207.2%20%5Ctimes%2010%5E%7B-4%7D%5C%5C%5C%5C%5Ctext%7BCheck%20for%20negligibility%20of%20%7Dx%5C%5C%5C%5C%5Cdfrac%7B2.7%7D%7B7.2%20%5Ctimes%2010%5E%7B-4%7D%7D%20%3D%204000%20%3E%20400%5C%5C%5C%5C%5Ctherefore%20x%20%5Cll%202.7%5C%5C%5Cdfrac%7Bx%5E%7B2%7D%7D%7B2.7%7D%20%3D%207.2%20%5Ctimes%2010%5E%7B-4%7D%5C%5C%5C%5Cx%5E%7B2%7D%20%3D%202.7%20%5Ctimes%207.2%20%5Ctimes%2010%5E%7B-4%7D%20%3D%201.94%20%5Ctimes%2010%5E%7B-3%7D%5C%5Cx%20%3D%200.0441%5C%5C%5Ctext%7B%5BH%24_%7B3%7D%24O%24%5E%7B%2B%7D%24%5D%7D%3D%20%5Ctext%7Bx%20mol%24%5Ccdot%24L%24%5E%7B-1%7D%24%7D%20%3D%20%5Ctext%7B0.0441%20mol%24%5Ccdot%24L%24%5E%7B-1%7D%24%7D)
2. Calculate the pH
![\text{pH} = -\log{\rm[H_{3}O^{+}]} = -\log{0.0441} = \large \boxed{\mathbf{1.36}}](https://tex.z-dn.net/?f=%5Ctext%7BpH%7D%20%3D%20-%5Clog%7B%5Crm%5BH_%7B3%7DO%5E%7B%2B%7D%5D%7D%20%3D%20-%5Clog%7B0.0441%7D%20%3D%20%5Clarge%20%5Cboxed%7B%5Cmathbf%7B1.36%7D%7D)
3. Calculate [C₆H₅O⁻]
C₆H₅OH + H₂O ⇌ C₆H₅O⁻ + H₃O⁺
2.7 x 0.0441
The correct answer is option a, that is, they produce ions when dissolved in water.
The acids and bases refer to the chemical components, which reacts with water. The molecules of acids dissociate to give hydrogen ions to water, while the bases dissociate to provide hydroxide ions to the water, or that takes hydrogen ions from water and leave the hydroxide ions behind.
1) (C2H5)2CBrCH2CH3 is the answer
explaiation:-
so when HBr is added to an alkene , according to the Markonicoff's rule ...H atoms are bonded to the C containing the most amount of H and Br is added to the other C.
2) Just add alkoholic KOH∆
Answer: (Structure attached).
Explanation:
This type of reaction is an aromatic electrophilic substitution. The overall reaction is the replacement of a proton (H +) with an electrophile (E +) in the aromatic ring.
The aromatic ring in p-fluoroanisole has two sustituents, an <u>halogen</u> and a <u>methoxy group</u>, which are <em>ortho-para</em> directing substituents.
Aryl sulfonic acids are easily synthesized by an electrophilic substitution reaction aromatic using <u>sulfur trioxide as an electrophile</u> (very reactive).
The reaction occurs in three steps:
- The attack on the electrophile forms the sigma complex.
- The loss of a proton regenerates an aromatic ring.
- The sulfonate group can be protonated in the presence of a strong acid (H₂SO₄).
Normally, a mixture of <em>ortho-para</em> substituted products would be obtained. However, since both <em>para</em> positions are occupied, only the <em>ortho </em>substituted product is obtained here.
