CHp. 12 Flashcards

1
Q

always contains carbon and hydrogen atoms.

may also contain other nonmetals such as oxygen, sulfur, nitrogen, phosphorus, or a halogen.

is often found in common products such as gasoline, medicines, shampoos, plastics, and perfumes.

A

organic

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2
Q

have covalent bonds.

have low melting and boiling points.
are flammable and undergo combustion.

are not soluble in water

A

organic

It burns easily in air

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3
Q

tetrahedral bond angle (or found single covalnet bonds)

A

109

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4
Q

all bonds are single

A

saturated

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5
Q

Alkane

A

Cn H2n+2

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6
Q

Cycloalkane

A

Cn H2n

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7
Q

have the same molecular formula with a different arrangements of atoms.
have the same number of atoms bonded in a different order

A

Structural isomers

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8
Q

groups of carbon atoms attached to carbon chains

named in the IUPAC system with a yl ending

A

alkyl

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9
Q

halogen atoms attached to the carbon chain.

named in the IUPAC system as fluoro, chloro, bromo, or iodo

A

halo substituents

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10
Q

Alkanes with ___ carbons are gases at room temperature and are widely used as heating fuels.

A

one to four

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11
Q

Alkanes with ____ carbons are highly volatile liquids at room temperature, which makes them useful as fuels

A

five to eight

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12
Q

weak attractions between nonpolar molecules. Caused by temporary dipoles that develop when molecules bump into each other weak but make it possible for nonpolar molecules to form liquids/solids

A

Dispersion forces

(aka london forces, van der Waals forces)

Common with carbon chains. VERY shortlived/instantaneous

Explains a higher boiling with longer CH chains

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13
Q

Lowest melting/boiling points of organic compounds

A

alkanes

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14
Q

contain only nonpolar bonds of CC, CH

A

alkanes

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15
Q

exhibit only weak dispersion forces in the solid and liquid states

A

alkanes

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16
Q

____-chain alkanes have more dispersion forces.

A

Longer

17
Q

have lower boiling points than the straight-chain isomers.

A

Branched alkanes

18
Q

tend to be more compact, reducing the points of contact between the molecules.

A

Branched alkanes

19
Q

do not have linear shapes and cannot line up close to each other

A

Branched alkanes

20
Q

have higher boiling points than the straight-chain alkanes with the same number of carbon atoms.

have limited rotation of carbon bonds; they maintain their rigid structure and can be stacked closely together, which gives them many points of contact and attractions to each other

A

cycloalkanes

21
Q

nonpolar.

insoluble in water.

less dense than water.

flammable in air.

found in crude oil

A

alkanes

22
Q

called unsaturated hydrocarbons because they do not contain the maximum number of hydrogen atoms

A

Alkenes and Alkynes

23
Q

react with hydrogen gas to increase the number of hydrogen atoms and become alkanes

A

Alkenes and Alkynes

24
Q

Each carbon atom in the double bond is attached to two hydrogen atoms and has a ___ arrangement with bond angles of 120

A

trigonal planar

25
Q

rigid and does not rotate

holds attached groups in fixed positions

makes cis–trans isomers (geometric isomers) possible when two different groups are attached to the carbon atoms on each side of the double bond

A

alkene

26
Q

undergo polymerization at high temperatures and pressure

easily broken, providing electrons to form new bonds

A

alkenes and alkynes, the double and triple bonds

27
Q

hydrogen atoms add to the carbon atoms of a double bond or triple bond.

a catalyst such as Pt, Ni, or Pd is used to speed up the reaction

A

Hydrogenation

28
Q

Vegetable oils are unsaturated fats composed of fatty acids that contain ___ bonds

A

double

29
Q

In hydration reactions, an alkene reacts with water, H—OH, to form an ____

A

alcohol

30
Q

A hydrogen atom (H—) from water forms a bond with the carbon atom in the double bond with ___ hydrogen atoms.

The—OH from water forms a bond with the second carbon atom in the double bond with ____ hydrogen atoms

(hydration rxn)

A

more

fewer

31
Q

an aromatic compound

a ring of six C atoms, each bonded to one H atom.

a flat ring structure drawn with three alternating double bonds.

represented by two structures, because the electrons are shared equally among all the C atoms.

represented by a line-angle structural formula using a circle in the center instead of the alternating double bonds

A

Benzene

32
Q

Benzene + methyl

A

toulene

33
Q

benzene + NH2

A

aniline

34
Q

benzene + OH

A

phenol

35
Q

two methyl groups + benzene

A

xylene