In order to extract isobutyric acid from a solution of diethyl ether, one should wash the solution with:
A. one 30mL wash of water
B. three 10mL washes of water
C. one 30mL wash of hexane
D. three 10mL washes of hexane
Answer
647.7k+ views
Hint: To solve this question, let’s first understand the properties of carboxylic acids. In case of simple aliphatic carboxylic acids, with four carbon atoms it is miscible in water due to the formation of hydrogen bonds with water. Solubility decreases by increasing the number of carbon atoms due to the increased hydrophobic interaction of the hydrocarbon part. Also, carboxylic acids are also soluble in less polar organic solvents.
Complete step by step answer:
As we know, isobutyric acid has a carboxylic acid group, which is polar and can readily hydrogen bond. It can be extracted from the organic solvent diethyl ether by washing with a polar solution like water. Multiple small volume washes extract better than one large volume wash. Use of a second organic solvent, hexane, will not extract the isobutyric acid from the diethyl ether. Now, we will consider all the four options.
A. One 30mL wash of water is incorrect as multiple smaller volume washes will yield higher extraction results.
B. Three 10mL washes of water is correct (option B) as isobutyric acid will enter the aqueous layer and wash off of the organic layer of diethyl ether.
C. One 30mL wash of hexane is also incorrect because hexane is another organic solvent like diethyl ether.
D. Three 10mL washes of hexane is also incorrect.
So, the correct answer is Option B.
Note:
We need to know that isobutyric acid is also known as 2-methylpropanoic acid or isobutyric acid. It is a carboxylic acid with structural formula ${(C{H_3})_2}CHCOOH$. It is an isomer of n-butyric acid. By deprotonation or esterification iso butyrates are formed.
Complete step by step answer:
As we know, isobutyric acid has a carboxylic acid group, which is polar and can readily hydrogen bond. It can be extracted from the organic solvent diethyl ether by washing with a polar solution like water. Multiple small volume washes extract better than one large volume wash. Use of a second organic solvent, hexane, will not extract the isobutyric acid from the diethyl ether. Now, we will consider all the four options.
A. One 30mL wash of water is incorrect as multiple smaller volume washes will yield higher extraction results.
B. Three 10mL washes of water is correct (option B) as isobutyric acid will enter the aqueous layer and wash off of the organic layer of diethyl ether.
C. One 30mL wash of hexane is also incorrect because hexane is another organic solvent like diethyl ether.
D. Three 10mL washes of hexane is also incorrect.
So, the correct answer is Option B.
Note:
We need to know that isobutyric acid is also known as 2-methylpropanoic acid or isobutyric acid. It is a carboxylic acid with structural formula ${(C{H_3})_2}CHCOOH$. It is an isomer of n-butyric acid. By deprotonation or esterification iso butyrates are formed.
Recently Updated Pages
If x a + bt + ct2 where x is in meters and t is in class 11 physics CBSE

A car covers the first half distance between two places class 11 physics CBSE

The resultant of two vectors overrightarrow P and overrightarrow class 11 physics CBSE

Find the value of cos 135 class 11 maths CBSE

A mass M is held in place by an applied force F and class 11 physics CBSE

A solution of glucose in water is labelled as 10 dfracwv class 11 chemistry CBSE

Trending doubts
One Metric ton is equal to kg A 10000 B 1000 C 100 class 11 physics CBSE

Find the value of the expression given below sin 30circ class 11 maths CBSE

What do you mean by retardation What is its SI uni class 11 physics CBSE

Draw a diagram of nephron and explain its structur class 11 biology CBSE

10 examples of friction in our daily life

Difference between physical and chemical change class 11 chemistry CBSE

