4a-Introduction Flashcards

1
Q

Q: What is a hydrocarbon?

A

A hydrocarbon is a compound that contains only hydrogen and carbon atoms. Examples include methane (CH₄), ethane (C₂H₆), and propane (C₃H₈).

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2
Q

Q: What are the different ways to represent organic molecules?

A

Organic molecules can be represented in several ways:

Empirical formula:
Molecular formula:
General formula:
Structural formula:
Displayed formula:

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3
Q

Empirical formula:

A

Shows the simplest ratio of atoms (e.g., CH₂ for ethene).

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4
Q

Molecular formula:

A

Shows the actual number of atoms (e.g., C₂H₄ for ethene).

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5
Q

General formula:

A

Represents an entire homologous series (e.g., alkanes: CₙH₂ₙ₊₂, alkenes: CₙH₂ₙ).

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6
Q

Structural formula:

A

Shows how atoms are arranged in a molecule (e.g., CH₃CH₃ for ethane).

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7
Q

Displayed formula:

A

Shows all atoms and bonds explicitly (e.g., ethene: H₂C=CH₂).

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8
Q

Q: What is a homologous series?

A

A homologous series is a family of organic compounds that:

Have the same general formula

Differ by a CH₂ unit between consecutive members

Show similar chemical properties

Have a gradual change in physical properties (e.g., boiling points increase with molecular size)

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9
Q

Q: What is a functional group?

A

A functional group is a specific group of atoms in a molecule responsible for its chemical reactions. Examples include:

Alkenes (-C=C-)

Alcohols (-OH)

Carboxylic acids (-COOH)

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10
Q

Q: What is isomerism?

A

Isomerism occurs when compounds have the same molecular formula but different structural arrangements.

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11
Q

Types of isomers : Structural isomerism

A

Structural isomerism: Different connectivity of atoms (e.g., butane vs. methylpropane)

Geometric (cis-trans) isomerism: Occurs in alkenes due to restricted rotation around the double bond

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12
Q

Types of isomers :
Geometric (cis-trans) isomerism:

A

Occurs in alkenes due to restricted rotation around the double bond

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13
Q

Q: How do you name organic compounds following IUPAC rules?

A

The IUPAC system follows these rules:

Identify the longest carbon chain (base name: methane, ethane, propane, etc.)

Identify and number the functional group (e.g., alcohol -OH at carbon 2 → propan-2-ol)

Identify and number any substituents (e.g., methyl, ethyl, chloro, etc.)

Arrange substituents alphabetically with the correct position numbers

Examples:

C₄H₁₀ (butane)

CH₃CH(CH₃)CH₃ (2-methylpropane)

CH₃CH=CH₂ (propene)

CH₃CH₂OH (ethanol)

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14
Q

Q: How do you write structural and displayed formulae?

A

A: Given a molecular formula, use these steps:

Identify the main chain and its functional group.

Draw the correct number of carbon and hydrogen atoms.

Include any functional groups or branching correctly.

Example:

Molecular formula: C₃H₆O

Possible structural formulae:

Propanal (CH₃CH₂CHO)

Propanone (CH₃COCH₃)

Displayed formula: Shows all bonds explicitly

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15
Q

How are organic reactions classified?A: Organic reactions three main types:

Substitution Reactions:

A

Substitution Reactions:

One atom or group is replaced by another.

Example: CH₄ + Cl₂ → CH₃Cl + HCl (Methane reacts with chlorine under UV light.)

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16
Q

How are organic reactions classified?A: Organic reactions three main types:

Addition Reactions:

A

Addition Reactions:

A reactant is added to a molecule without removing any atoms.

Example: C₂H₄ + Br₂ → C₂H₄Br₂ (Ethene reacts with bromine, confirming the presence of a double bond.)

17
Q

How are organic reactions classified?A: Organic reactions three main types:
Combustion Reactions:

A

Hydrocarbons react with oxygen to produce CO₂ and H₂O (complete combustion) or CO and H₂O (incomplete combustion).

Example:

Complete combustion: CH₄ + 2O₂ → CO₂ + 2H₂O

Incomplete combustion: CH₄ + O₂ → CO + 2H₂O