Organic Chemistry - SS1 Chemistry Past Questions and Answers - page 4
Which functional group is commonly found in esters and is responsible for their fruity odour?
Hydroxyl
Carbonyl
Carboxyl
Ester
Which functional group is commonly found in ethers and is responsible for their low boiling points?
Thiol
Carbonyl
Ether
Amide
What are functional groups, and why are they important in organic chemistry?
Functional groups are specific groups of atoms within organic molecules that determine their chemical properties and reactivity. They play a crucial role in organic chemistry because they define the behaviour and reactions of organic compounds. By identifying and understanding functional groups, chemists can predict the properties, reactions, and intermolecular interactions of organic molecules, facilitating the synthesis of new compounds and the understanding of their biological activities.
Discuss the properties and reactivity of the hydroxyl functional group.
The hydroxyl functional group (-OH) is characterised by the presence of an oxygen atom bonded to a hydrogen atom. It imparts several important properties to organic compounds. The hydroxyl group is polar, making compounds containing it capable of forming hydrogen bonds with other molecules or functional groups. This leads to higher boiling points, solubility in water, and increased intermolecular forces. The presence of a hydroxyl group also renders compounds capable of acidic or basic behaviour, depending on the surrounding functional groups. Additionally, the hydroxyl group can participate in various chemical reactions, such as dehydration to form ethers, esterification to form esters, and oxidation to form aldehydes or carboxylic acids.
Explain the significance of the carbonyl functional group in organic chemistry.
The carbonyl functional group (C=O) is one of the most important and versatile functional groups in organic chemistry. It consists of a carbon atom doubly bonded to an oxygen atom. The presence of the carbonyl group imparts distinctive properties and reactivity to organic compounds. It gives rise to the polarity of the C=O bond, making compounds containing it more reactive towards nucleophiles. The carbonyl group is responsible for several important classes of organic compounds, including aldehydes, ketones, carboxylic acids, and esters. It participates in reactions such as nucleophilic addition, condensation, and oxidation-reduction reactions. The carbonyl group also plays a vital role in biological processes, such as enzymatic catalysis and the formation of peptide bonds in proteins.
Isomerism refers to:
The presence of different functional groups in a compound.
The existence of multiple carbon atoms in a molecule.
The phenomenon where two or more compounds have the same molecular formula but different structural arrangements or spatial orientations.
The ability of a compound to exist in different physical states.
Which of the following is an example of structural isomerism?
Ethanol and methanol
Propanol and propanal
Cyclohexane and hexane
Glucose and fructose
Ethanol and methanol
Propanol and propanal
Cyclohexane and hexane
Glucose and fructose
Geometric isomerism is commonly observed in compounds with:
Double bonds
Triple bonds
Aromatic rings
Halogen atoms
Optical isomerism arises due to:
Different arrangements of carbon atoms in a molecule.
Different spatial arrangements of atoms around a chiral centre.
The presence of multiple functional groups in a compound.
The presence of a triple bond in a molecule.
Which of the following is an example of tautomeric isomerism?
Glucose and fructose
Ethanol and ethanoic acid
Acetaldehyde and acetone
Butane and 2-methylpropane