intro to organic chem Flashcards

1
Q

How many electrons are shared in a double bond, e.g. C=C in ethene?

A

Four

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2
Q

What is the bond angle in methane?

A

109.5o

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3
Q

Define empirical formulae.

A

The simplest whole number ratio in which the atoms of each element are present in a compound.

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4
Q

Define molecular formula.

A

A formula that tells us the actual number of atoms of each different element that makes up a molecule.

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5
Q

Define structural formula.

A

A formula showing the atoms present in a molecule and how they are joined together.

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6
Q

What does a displayed formula show?

A

A displayed formula shows all the atoms in a compound and their bonds.

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7
Q

What is a hydrocarbon?

A

A compound containing only hydrogen and carbon atoms.

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8
Q

Define functional group.

A

An atom, or group of atoms, in a molecule which determines its chemical properties.

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9
Q

What are the three characteristics of a homologous series?

A
  • Same general formula
  • Same functional group
  • Same chemical reactivity
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10
Q

What is the general formula for an alkane?

A

CnH2n+2

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11
Q

What is the general formula for an alkene?

A

CnH2n

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12
Q

Define structural isomerism.

A

Two or more compounds with the same molecular formula but different structural formulae.

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13
Q

State, describe and give examples of the three different types of structural isomerism.

A
  1. Chain isomerism: two isomers with the same molecular formula but a different arrangement of carbon chain. For example, butan-1-ol and 2-methylpropan-1-ol.
  2. Positional isomerism: two isomers with the same molecular formula but the functional group is attached to different points of the main carbon chain. For example, 1-bromopropane and 2-bromopropane.
  3. Functional group isomerism: two isomers with the same molecular formula but a different functional group. For example: C5H10 can be both pentene and cyclopentane.
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14
Q

Define the term stereoisomer.

A

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

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15
Q

Explain why alkenes show E-Z isomerism but alkanes do not.

A

Alkenes contain a double bond that is planar and unable to rotate. Therefore, the substituent groups are locked in place and E-Z isomerism can arise. Alkanes contain only single covalent bonds that are able to rotate and, therefore, E-Z isomerism cannot occur.

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