Ch 7 A - Structure of Organic Compounds Flashcards

1
Q

what properties of carbon allow it to bond to a variety of atoms

A
  • its valence electron number
  • relative bond strength
  • relative stability of carbon bonds with other elements.
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2
Q

number and uses of carbons valence electrons

A

4 valence electrons
-Each carbon atom
forms four bonds in a tetrahedral arrangement
- carbon is able to form either single, double, or triple bonds
with either itself or other elements

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3
Q

factors that impact the energy of chem bond

A

bond length
* the difference in electronegativity of the atoms involved
* size of the atoms.

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4
Q

bond length

A

distance between the nuclei of two bonded atoms

vary depending on the strength of the
electrostatic attraction between the nuclei of the bonded atoms and their
shared electrons.

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5
Q

relation between bond length and energy

A

in general bond energy (and hence bond strength) increases as the length of a
bond decreases.

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6
Q

relationship between electronegativity and bond strength

A

bonds formed between elements with larger differences in electronegativity form stronger bonds

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7
Q

alkanes
general formula
general structure

A

saturated hydrocarbons that have only single
carbon-carbon bonds in their structures.
Cn H2n + 2

linear or branched
chains (due to the presence of side chains)

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8
Q

alkenes
general formula
general structure

A

unsaturated hydrocarbons - at least one c-c double bond

Cn H2n

double bond causes a kink in the carbon chain

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9
Q

cycloalkane

A

an alkane arranged in a closed
ring with no terminal carbon.
ie cyclohexane

each carbon atom is bonded to two
adjacent carbon atoms and two hydrogen atoms.

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10
Q

branched alkanes general formula

A

Cn H2n

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11
Q

Cyclohexane and benzene are

A

hydrocarbons with a cyclic structure.

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12
Q

Benzene

A

cyclic compound
- 6 carbon atoms in its ring structure,
each bonded to one hydrogen atom and two adjacent carbon atoms. One electron
from each carbon atom is delocalised and shared equally between carbon atoms
in the ring, resulting in a very stable formation

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13
Q

Haloalkanes

A

are alkane-based compounds that have one or more halogen atoms
bonded to the carbon chain(in place of hydrogens)

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14
Q

why do haloalkanes have a polar bond

A

more electronegative than carbon atoms
- tendency to attract
the shared pair of electrons to their own nucleus.
- polar bond
carbon atom has a partial positive charge
- halogen atom has a partial negative charge

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15
Q

Amine 

A

organic compound with an amino functional group (−NH2)

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16
Q

Alkyl group 

A

group containing only carbon and hydrogen atoms (e.g. −CH3, −CH2CH3)

17
Q

Amide functional groups

A

(−CONH)
contains a carbonyl group (C=O) whose carbon atom is bonded to
a nitrogen atom

18
Q

Primary amide 

A

organic compound that contains an amide functional group at a terminal carbon atom (−CONH2)

nitrogen is only bonded to one carbon - hence found at terminal carbon

19
Q

Alcohols

A

derivatives of hydrocarbons that have a hydroxyl (−OH) group bonded to a carbon atom in the carbon chain.

OH in place of a H

20
Q

primary, secondary, and tertiary alcohols

A

carbon that is bonded to OH, is also bonded to one, two and three alkyl groups respectively

21
Q

Aldehydes and ketones

A

are compounds that have a carbonyl group (C=O) in
their structures

carbon in the carbonyl group is able to take part in two more covalent bonds.

22
Q

Aldehydes

A

one remaining carbon bonds with hydrogen, forming (-CHO) functional group.
only exists at the end of a carbon chain.
The carbon atom can then either bond with a hydrogen atom or an alkyl group.

23
Q

ketones

A

organic compound that contains a carbonyl functional group (C=O), where the
carbon atom in the −C=O group is bonded to two other carbon atoms (aka alkyl groups)

24
Q

Carboxyl group 

A

a combination of hydroxyl (−OH) and carbonyl (C=O) groups functional groups (−COOH) attached to a single carbon atom

found at the
end of the carbon chain

may either bond to an
alkyl group or a hydrogen atom

25
Q

why are carboxyl’s weak acids

A

has the capacity to donate its H+ into
a solution, it is able to act as a weak acid.

26
Q

ester

A

organic compound that contains an ester functional group (−COOC−)

one carbon
atom is linked to one oxygen atom through a double bond
(a carbonyl) and to another oxygen atom through a single bond.
The oxygen atom
in the single carbon-oxygen bond is then bonded to an alkyl group