3.3.1 Intro to organic chemistry Flashcards

Apply systematic nomenclature and structural representations to classify organic compounds and reaction mechanisms. (42 cards)

1
Q

What is the simplest whole-number ratio of atoms of each element in a compound called?

A

Empirical formula

It shows the simplest ratio of atoms present.

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2
Q

What formula shows the actual number of atoms of each element in a molecule?

A

Molecular formula

For example, glucose has molecular formula C6H12O6.

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3
Q

Fill in the blank:

A formula showing the arrangement of atoms and bonds in a molecule is called the _______ formula.

A

structural

It indicates how atoms are connected.

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4
Q

True or False:

A displayed formula shows every atom and bond in a molecule.

A

True

All covalent bonds are shown explicitly.

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5
Q

What type of formula uses lines to represent carbon–carbon bonds and omits most hydrogen atoms?

A

Skeletal formula

Carbon atoms are implied at the ends and intersections of lines.

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6
Q

True or False:

Skeletal formulas normally show all hydrogen atoms attached to carbon.

A

False

Hydrogens attached to carbon are usually omitted.

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7
Q

Fill in the blank:

A family of organic compounds with the same functional group is called a _______ series.

A

homologous

Members differ by a repeating –CH2– unit.

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8
Q

What feature is common to all members of a homologous series?

A

Same functional group

This leads to similar chemical reactions.

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9
Q

True or False:

Members of a homologous series show a gradual change in physical properties.

A

True

For example, boiling point increases with chain length.

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10
Q

What naming system is used internationally for naming organic compounds?

A

IUPAC nomenclature

The International Union of Pure and Applied Chemistry sets the rules.

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11
Q

Fill in the blank:

In IUPAC naming, the longest continuous chain of carbon atoms determines the _______ name.

A

parent

The parent chain forms the base name of the compound.

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12
Q

According to A-level requirements, organic compounds should be named using chains of up to how many carbon atoms?

A

Six

Students must apply IUPAC rules to chains and rings up to six carbons.

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13
Q

What term describes the step-by-step pathway showing how reactants form products in an organic reaction?

A

Reaction mechanism

It shows the movement of electrons and formation/breaking of bonds.

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14
Q

What type of species has an unpaired electron and is involved in certain organic reactions?

A

Radical

Radicals are highly reactive species with a single unpaired electron.

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15
Q

Fill in the blank:

In radical mechanisms, the unpaired electron is represented by a _______.

A

dot

A dot next to the atom symbol shows the radical.

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16
Q

True or False:

Curly arrows are normally used to show electron movement in free-radical mechanisms.

A

False

Radical mechanisms usually use single dots rather than curly arrows.

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17
Q

What type of arrow is used to show the movement of an electron pair in many organic mechanisms?

A

Curly arrow

The arrow starts at the electron pair and points to where the electrons move.

18
Q

True or False:

A curly arrow can start from a lone pair of electrons to show bond formation.

A

True

This represents donation of an electron pair to form a covalent bond.

19
Q

Fill in the blank:

When a covalent bond breaks in a mechanism, the curly arrow starts from the _______.

A

bond

This indicates the electrons move away from that bond.

20
Q

What does a curly arrow represent in an organic reaction mechanism?

A

Movement of an electron pair

It shows how electrons rearrange during the reaction.

21
Q

True or False:

Reaction mechanisms must show the structures of all species involved in each step.

A

True

Each intermediate and transition step should be represented.

22
Q

What must be written for each step in a free-radical mechanism besides structures?

A

Balanced equation

Each stage (initiation, propagation, termination) must balance atoms.

23
Q

Fill in the blank:

The formation of a new covalent bond occurs when an electron _______ is shared between atoms.

A

pair

Curly arrows illustrate this movement of electron pairs.

24
Q

Why are mechanisms useful in organic chemistry?

A

Explains how reactions occur.

They show the detailed sequence of bond breaking and bond forming.

25
What term describes **compounds with the same molecular formula** but different **structural arrangements**?
Isomers ## Footnote Isomers share a formula but differ in structure or spatial arrangement.
26
What type of **isomerism** occurs when **atoms are connected in different ways** within molecules?
Structural isomerism ## Footnote These isomers differ in the arrangement of atoms in the molecule.
27
# Fill in the blank: **Structural isomers** have the same molecular formula but different _\_\_\_\_\_\_ formulas.
structural ## Footnote The atoms are connected differently.
28
# True or False: **Chain isomerism** occurs when the **carbon skeleton differs** between molecules.
True ## Footnote For example, straight-chain vs branched-chain hydrocarbons.
29
What type of **structural isomerism** occurs when the **functional group** is located in different positions?
Position isomerism ## Footnote The carbon skeleton remains the same but the group moves position.
30
# True or False: **Functional group isomers** have the same functional group but in different positions.
False ## Footnote Functional group isomers contain different functional groups.
31
# Fill in the blank: Isomers that differ only in the **spatial arrangement of atoms** are called _\_\_\_\_\_\_ isomers.
stereoisomers ## Footnote The bonding arrangement remains the same.
32
What type of **stereoisomerism** occurs due to **restricted rotation around a C=C double bond**?
E–Z isomerism ## Footnote The double bond prevents free rotation of substituents.
33
# True or False: **E–Z isomerism** can occur around **single carbon–carbon bonds**.
False ## Footnote Single bonds rotate freely so stereoisomerism does not occur.
34
# Fill in the blank: The system used to assign **priorities** when determining E or Z configuration is the _\_\_\_\_\_\_ rules.
CIP ## Footnote Cahn–Ingold–Prelog priority rules determine substituent ranking.
35
In **E–Z notation**, what does the letter **E** indicate about the highest priority groups?
Opposite sides ## Footnote E comes from the German “entgegen,” meaning opposite.
36
In **E–Z notation**, what does the letter **Z** indicate about the highest priority groups?
Same side ## Footnote Z comes from the German “zusammen,” meaning together.
37
What is the functional group isomer of an **aldehyde**?
A ketone
38
What is the functional group isomer of a **ketone**?
An aldehyde
39
What is the functional group isomer of an **alcohol**?
An ether
40
What is the functional group isomer of an **ether**?
An alcohol
41
What is the functional group isomer of a **carboxylic acid**?
An ester
42
What is the functional group isomer of an **ester**?
A carboxylic acid