The skeletal structure of an organic compound is an abbreviated representation of its molecular structure, they are quick and easy to draw.
For example, the following image shows the skeletal structure of a compound:
The peaks represent the carbons. We must remember that carbon can have a maximum of 4 bonds.
Now, I will show you how is the structure of this specific compound:
This is ternary alcohol, called 2-methyl-2-butanol. If you see carefully, you will notice that each carbon has 4 bonds. The functional groups present will be OH. The skeletal structure will be:
Answer : 17.12 g
Explanation:
= elevation in boiling point
= boiling point elevation constant
m= molality
given 
Molar mass of solute = 46.0 
Weight of the solvent = 150.0 g = 0.15 kg
Putting in the values
x = 17.12 g
Answer:
Correct answer is (D). as a weak acid it can cross the membrane when in its uncharged form.
Explanation:
Aspirin (acetylsalicylic acid, ASA) is an analgesic and anti-inflammatory agent use in the treatment of gentle to moderate pain, inflammation and fever. It is absorb in the stomach and intestine in an unchanged form.
Answer:
3.6 × 10⁻⁵ M
Explanation:
Ergosterol has a maximum absorbance at λ = 282 nm. The absorbance of an analyte is related to its concentration through the Beer-Lambert's law.
A = ε × <em>l</em> × c
where,
A: absorbance
ε: molar absorptivity
<em>l</em>: optical path length
c; molar concentration
c = A / ε × <em>l </em>= 0.43 / (11,900 M⁻¹cm⁻¹) × 1.00 cm = 3.6 × 10⁻⁵ M
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