Module 4: Alkenes Flashcards

1
Q

Define sigma bond

A

A bond formed by the lengthways overlap of orbitals directly between two bonding atoms.

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2
Q

Define Pi bond

A

A type of covalent bond formed when adjacent p-orbitals overlap sideways above and below the bonding c atoms.

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3
Q

What does the carbon-carbon double bond mean?

A

A bond formed between two carbon atoms that share two pairs of electrons.

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4
Q

Define structural isomerism.

A

Molecules with the same molecular formula but different structural arrangements of atoms.

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5
Q

What is stereoisomerism?

A

Molecules with the same structural formula but different arrangements of atoms in space.

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6
Q

What is one type of stereoisomerism?

A

Geometric isomerism.

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7
Q

When does stereoisomerism occur?

A

As a result of restricted rotation about the C=C double bond.

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8
Q

What is a cis isomer?

A

An isomer with the same groups on the same side.

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9
Q

What is a trans isomer?

A

An isomer with the same groups on either side.

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10
Q

What is the priority group?

A

The atom with the highest atomic number.

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11
Q

When are cis-trans isomers relevant?

A

When there are at least two of the same groups present.

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12
Q

Name the four types of reactions of alkenes.

A
  • Hydrogenation
  • Hydration
  • Halogenation (water)
  • Addition of an acid
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13
Q

Fill in the blank: The carbon-carbon double bond is represented as _______.

A

C=C

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14
Q

What is electrophilic addition?

A

A reaction where an electrophile reacts with a nucleophile to form a product

Electrophilic addition typically occurs with alkenes and alkynes.

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15
Q

What is an electrophile?

A

A species that accepts an electron pair

Electrophiles are often positively charged or neutral molecules with vacant orbitals.

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16
Q

What does the term ā€˜C=C’ signify?

A

A double bond between two carbon atoms

This notation indicates a pi bond and sigma bond between the two carbons.

17
Q

Explain electrophilic addition in alkenes.

A

Addition of electrophiles to the double bond of alkenes to form saturated products

This process results in the breaking of the C=C bond.

18
Q

What are the products formed in electrophilic addition reactions?

A

Saturated products

The reaction converts unsaturated hydrocarbons to saturated hydrocarbons.

19
Q

What attracts electrophiles to a double bond?

A

The high electron density of the double bond

The electron-rich area of the double bond interacts with electrophiles.

20
Q

Fill in the blank: Electrophiles have an atom with _______ charge.

21
Q

What happens to the C=C bond during electrophilic addition?

A

It breaks to form a new single bond

This allows for the addition of new atoms or groups to the molecule.

22
Q

What is a carbocation?

A

A positively charged carbon ion

Carbocations are key intermediates in many organic reactions, including electrophilic additions.

23
Q

How does a nucleophile interact with an electrophile in electrophilic addition?

A

The nucleophile donates a pair of electrons to the electrophile

This interaction forms new bonds and stabilizes the reaction intermediate.