Properties of Hydrocarbons and Functional Groups

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Flashcards covering electronegativity and bond types, molecular polarity, intermolecular forces, hydrophilicity versus hydrophobicity, hydrocarbon classes, alkane physical properties, and a wide range of common organic functional groups with their naming conventions.

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35 Terms

1
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What type of bond is formed when the electronegativity difference between two atoms is less than 0.5?

A non-polar covalent bond.

2
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At what electronegativity difference range is a bond considered polar covalent?

When the electronegativity difference is between 0.5 and 2.0.

3
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When the electronegativity difference exceeds about 2.0, what kind of bond is most likely?

An ionic bond.

4
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Are C–H bonds considered polar or non-polar?

Non-polar.

5
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What physical quantity measures overall molecular polarity?

Dipole moment (μ).

6
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How is the dipole moment of a molecule determined?

By the vector sum of all individual bond dipoles and lone-pair contributions.

7
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Why is CO2 non-polar even though it contains polar C=O bonds?

The two bond dipoles are equal and oriented in opposite directions, cancelling each other out.

8
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Give an example of a molecule with a net dipole despite having several identical polar bonds.

CHF3 (trifluoromethane) is polar because its bond dipoles do not cancel.

9
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What intermolecular force exists between all molecules, polar or non-polar?

London (dispersion) forces.

10
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Which intermolecular force arises from attractions among permanent dipoles of polar molecules?

Dipole-dipole forces.

11
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Define a hydrogen bond in organic chemistry.

An attractive interaction between a hydrogen bonded to an electronegative O or N and an unshared electron pair on another O or N.

12
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Give two biological examples where hydrogen bonding is crucial.

Maintaining enzyme shape and stabilising the DNA double helix.

13
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What does the term hydrophilic mean?

‘Water-loving’; substances that contain ionic charges or polar –OH groups and can hydrogen-bond with water.

14
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Why are alkanes classified as saturated hydrocarbons?

Every carbon in an alkane has the maximum possible number of hydrogens; all bonds are single.

15
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Name the four main classes of hydrocarbons.

Alkanes, alkenes, alkynes, arenes (aromatic hydrocarbons).

16
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How does the presence of a C=C double bond change the classification of a hydrocarbon?

It becomes an alkene (an unsaturated hydrocarbon).

17
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What general trend is observed for boiling and melting points of straight-chain alkanes as molecular weight increases?

Both boiling and melting points increase with increasing molecular weight.

18
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How does branching affect the boiling point of an alkane?

More branching lowers the boiling point because of decreased surface area and weaker dispersion forces.

19
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Are alkanes soluble in water? Why or why not?

No; alkanes are non-polar and cannot form strong interactions with polar water molecules.

20
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State the ‘like dissolves like’ principle using alkanes as an example.

Non-polar alkanes dissolve in other non-polar solvents (e.g., toluene or diethyl ether) but not in polar solvents like water.

21
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What is a functional group?

An atom or group of atoms within a molecule that shows a characteristic set of predictable physical and chemical behaviours.

22
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List four reasons functional groups are important in organic chemistry.

They determine chemical reactivity, influence physical properties, provide a basis for classification, and form the foundation for systematic nomenclature.

23
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Which functional group defines alcohols?

The hydroxyl group (–OH) attached to a saturated carbon.

24
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What suffix is used in IUPAC names for alkenes?

-ene.

25
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What functional group characterises aldehydes?

A carbonyl group bonded to at least one hydrogen (-CHO).

26
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Which suffix indicates a ketone in IUPAC nomenclature?

-one.

27
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Give the functional group and suffix for carboxylic acids.

Carboxyl group (-COOH); suffix “-oic acid.”

28
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What functional group is present in an ester?

A carbonyl carbon bonded to an OR group (-COOR).

29
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How are amides structurally identified?

A carbonyl carbon bonded to a nitrogen (-CONR2).

30
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What suffix is assigned to nitriles?

-nitrile (or ‑carbonitrile).

31
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Define an amine and give its naming suffix.

A compound with one or more alkyl groups attached to nitrogen; suffix “-amine.”

32
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What functional group is characteristic of sulfides?

A sulfur atom singly bonded to two carbon atoms (R-S-R).

33
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Which functional group contains an S–S bond?

Disulfides (R-S-S-R).

34
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What is the difference between a thiol and an alcohol?

In a thiol the oxygen of an alcohol is replaced by sulfur (R-SH).

35
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Give the functional group found in sulfoxides.

A sulfur doubly bonded to oxygen and singly bonded to two carbons (R-S(=O)-R).