Chemistry · Organic chemistry: basic principles and techniques · chapter 8 of 9

Class 11 Chemistry Chapter 8: Organic Chemistry – Some Basic Principles and Techniques MCQs with answers

10 multiple-choice questions on Organic Chemistry – Some Basic Principles and Techniques, each with its answer and the reason, written from the NCERT chapter. For school exams on the CBSE pattern, JEE Main and NEET, which are set from the same NCERT chapter. Open a question's solution to check your working; then take the free test to find your next chapter.

Question 1
Wöhler's synthesis of urea, which ended the vital-force idea, started from the inorganic compound
Show answer

Answer: (c) ammonium cyanate

Wöhler heated ammonium cyanate: NH₄CNO → NH₂CONH₂. The other three are inorganic salts, but not the one he used.

Question 2
In which molecule are all the carbon atoms in the same hybridisation state?
Show answer

Answer: (a) CH₂=CH–CH=CH₂

Each carbon of CH₂=CH–CH=CH₂ forms one double bond, so all four are sp². In CH₂=C=CH₂ the middle carbon (two double bonds) is sp and the ends sp²; CH₃–C≡CH has sp³ and sp; CH₂=CH–C≡N has sp² and sp.

Question 3
The numbers of σ and π bonds in a molecule of propenal, CH₂=CH–CHO, are
Show answer

Answer: (b) 7 σ and 2 π

σ bonds: C=C (1), C–C (1), C=O (1) and four C–H, total 7. π bonds: one in C=C and one in C=O, total 2. 6 σ forgets the aldehyde C–H; 3 π counts the C–C single bond as a π bond.

Question 4
In the direct estimation of oxygen, 0.30 g of an organic compound finally gave 0.44 g of carbon dioxide (after the CO is oxidised by I₂O₅). The percentage of oxygen in the compound is
Show answer

Answer: (d) 53.3%

Each mole of O₂ in the compound gives 2 mol CO₂, so 88 g CO₂ comes from 32 g O₂. % O = (32 × 0.44 × 100)/(88 × 0.30) = 53.3%. Using 44 g gives an impossible 106.7%; 40.0% is the carbon fraction 12/44; 26.7% halves the right answer.

Question 5
The carbon atom is the most electronegative in
Show answer

Answer: (a) HC≡CH

Electronegativity of carbon rises with the s character of its hybrid orbitals. The sp carbon of ethyne has 50% s character, more than sp² (33%) or sp³ (25%).

Question 6
A bond-line formula is a zig-zag of four line segments with =O drawn on the second point from one end, and nothing else written. The compound is
Show answer

Answer: (d) pentan-2-one

Four segments have five points, each a carbon; the ends are CH₃ groups. The C=O on the second carbon makes it CH₃COCH₂CH₂CH₃, pentan-2-one. Butan-2-one counts segments instead of points; pentanal would need the O at an end.

Question 7
In a wedge-and-dash formula, a bond drawn as a solid wedge shows a bond that
Show answer

Answer: (b) projects out of the plane of the paper, towards the observer

A solid wedge points towards the observer, its broad end nearer; a dashed wedge points away; a plain line lies in the plane.

Question 8
A molecular model in which no bonds are shown and each atom is drawn to its van der Waals size, so that the volume the molecule occupies is seen, is the
Show answer

Answer: (c) space-filling model

The space-filling model shows the relative size of each atom from its van der Waals radius and no bonds. The framework model shows only bonds; ball-and-stick and ball-and-spring show both atoms and bonds.

Question 9
Tetrahydrofuran is a five-membered ring of four CH₂ groups and one oxygen atom. It is classified as
Show answer

Answer: (d) a heterocyclic alicyclic (non-aromatic) compound

Its ring holds an atom other than carbon, so it is heterocyclic, and it is saturated, so it is alicyclic, not aromatic. Furan, its unsaturated relative, is the heterocyclic aromatic one.

Question 10
The IUPAC name of CH₃–CH(CH₃)–CH₂–CH(C₂H₅)–CH₂–CH₃ is
Show answer

Answer: (a) 4-ethyl-2-methylhexane

The longest chain has six carbons. Numbering from the left puts the branches at 2 and 4 (from the right, 3 and 5), so 2 and 4. Ethyl is written before methyl in alphabetical order: 4-ethyl-2-methylhexane. Option c breaks the alphabetical order; option d does not use the longest chain.

Take the free Class 11 Chemistry testSee the Class 11 flashcards

← Chapter 7: Redox ReactionsChapter 9: Hydrocarbons →