Chemistry Exam 3

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chapter 9 - 13

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39 Terms

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Alcohol

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Ether

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Aldehyde

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Ketone

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Carboxylic Acid

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Ester

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Amide

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Amine

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Methane

CH4

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Ethane

C2H6

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Propane

C3H8

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Butane

C4H10

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Pentane

C5H12

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Hexane

C6H14

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Heptane

C7H16

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Octane

C8H18

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Nonane

C9H20

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Decane

C10H22

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London Dispersion Force (LDF)

  • larger cloud = stronger force

  • more surface area = stronger force

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dipole-dipole

  • greater separation of positive and negative charges = stronger attractions

  • orientation: positive end needs to attract a negative end

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dipole induced dipole

  • stronger dipole moment = stronger force

  • larger atom = stronger force (more polarizable)

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ion induced dipole

  • higher charges = stronger forces

  • larger atoms = stronger forces (more polarizable)

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ion-ion

  • greater charge = stronger force

  • closer together = stronger interaction

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High melting and boiling point

stronger IMFs; more energy is required to break the interaction

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Low melting and boiling point

weak IMFs; less energy needed to overcome the forces

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Polarizability

how easily an electron cloud can be distorded

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induced dipole

a temporary dipole created in a nonpolar molecule due to an external electric field or nearby charge; causes the electron cloud to shift and creates a region of partial positive charge and a region of partial negative charge

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Solids

Molecular Structure: closely packed, don’t freely move

IMF: strongest, keep molecules in a fixed shape and volume

KE: low

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Liquids

Molecular Structure: close but not fixed arrangement

IMF: weaker but strong enough to keep molecules near each other; allows for a defined volume but not a fixed shape

KE: molecules can partially overcome IMF enabling movement but not seperation

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Gases

Molecular Structure: far apart in constant random motion

IMF: weak and often negligible

KE: high, allowing to completely overcome IMF allows free movement in all directions

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Intramolecular Force

forces that hold atoms together within a molecule forming chemical bonds

  • covalent, ionic, and metallic bonds

breaking requires a chemical reaction and are in the range of 100-1000 kJ/mol

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Intermolecular Force (IMF)

forces of attraction between separate molecules

  • LDR, Dipole-Dipole, hydrogen bonds

determine physical changes rather than breaking apart

  • forces range from 1-50 kJ/mol

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Alkane

CnH2n+2

saturated with single bonds

  • strong and nonpolar

  • combustion and substitution reactions

  • high stability

<p><strong>C<sub>n</sub>H<sub>2n+2</sub></strong></p><p>saturated with single bonds </p><ul><li><p>strong and nonpolar</p></li><li><p>combustion and substitution reactions</p></li><li><p>high stability</p></li></ul><p></p>
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Alkene

CnH2n

Unsaturated with at least one double bond

  • addition reactions

  • less stable than alkanes

<p><strong>C<sub>n</sub>H<sub>2n</sub></strong></p><p>Unsaturated with at least one double bond</p><ul><li><p>addition reactions</p></li><li><p>less stable than alkanes</p></li></ul><p></p>
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Alkyne

CnH2n-2

Unsaturated with at least one triple bond

  • addition reactions

  • less stable than alkenes and alkanes

<p><strong>C<sub>n</sub>H<sub>2n-2</sub></strong></p><p>Unsaturated with at least one triple bond</p><ul><li><p>addition reactions</p></li><li><p>less stable than alkenes and alkanes</p></li></ul><p></p>
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Aromatic

a ring of carbon atoms with alternating single and double bonds

  • electrophilic substitution reactions

  • high stability makes them less reactive

<p>a ring of carbon atoms with alternating single and double bonds</p><ul><li><p>electrophilic substitution reactions</p></li><li><p>high stability makes them less reactive</p></li></ul><p></p>
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Isomer

a molecule that shares the same molecular formula as another molecule but differs in the arrangement

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Geometric Isomer

some molecular formula and some connectivity but different arrangements

  • look for restricted rotation (double bonds or rings)

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Constitutional Isomer

same molecular formula but atoms are connected differently

  • atoms bonded in different orders