Organic chemistry Flashcards

1
Q

Define molecular formula

A

expresses the exact composition of a molecule or substance

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2
Q

define empirical formula

A

the simplest whole number ratio of atoms of each element in a compound

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3
Q

define heteroatom

A

any atom which is not carbon or hydrogen

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4
Q

define constitutioanl isomers

A

they vary in structure through their arrangement of atoms

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5
Q

what is the difference between the labels isopropyl and propyl

A

isopropyl is when the bond from the main carbon chain is connected to the middle carbon on the propyl chain, rather than the first

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6
Q

how do you name an ether

A

identify the shortest chain, put oxy on the end, end the word with the longest chain

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7
Q

what is the difference between an ether and an ester

A

an ether has an oxygen atom in the chain of carbons, but an ester has an oxygen in the chain, and the next carbon is connected to an oxygen via a double bond

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8
Q

define polar covalent bond

A

when two atoms are bonded covalently but they have significantly different electronegativities and so the more electronegative atom finds the pair of electrons closer to it

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9
Q

define electronegativity

A

the tendency of an atom to attract a shared pair of electrons towards itself

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10
Q

list all of the types of bonds from strongest to weakest

A

covalent, ionic, metallic, hydrogen, dipole-dipole, london dispersion

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11
Q

why do longer alkanes have a higher melting/boiling point than shorter ones

A

the longer the chain, the more attractive forces per molecule, meaning more energy is required to break the intermolecular forces

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12
Q

why do alkanes float on water

A

they are less dense, non-polar, and hydrophobic

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13
Q

what do alkanes form in their solid state

A

a wax

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14
Q

why do branched alkanes have lower melting and boiling points then their linear isomers

A

they have substituted chains which are not able to pack as efficiently

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15
Q

define conformations

A

the different arrangements of atoms in a molecule in space due to rotation

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16
Q

do eclipsed or staggered newman projections have higher energy

A

eclipsed as lower distance between the eclipsing atoms

17
Q

what are the three types of ring strain

A

angle - angles deviate from 109
torsional - methyl groups on adjacent carbons eclipsed
steric - methyl on non-adjacent carbons are too close

18
Q

define axial bonds

A

the six axial bonds, one on each carbon in a ring, are parallel and alternate up and down

19
Q

define equatorial bonds

A

the six equatorial bonds, one on each carbon in a ring, come in three sets of two parallel lines, they also alternate between sides around the ring

20
Q

are axial or equatorial bonds higher in energy

A

axial

21
Q

why are carbon-carbon sigma bonds stronger than carbon-carbon pi bonds

A

they are less susceptible to electrons

22
Q

why are there more trans isomers than cis

A

they are thermodynamically more stable due to steric strain existing in the cis form

23
Q

what is the difference between E and Z isomers

A

E - higher ranked groups are on opposite sides
Z - higher ranked groups are on the same side

24
Q

define stereoisomers

A

same atomic connectivity but differ in special arrangement of the constituent atoms

25
Q

define enantiomers (optical isomers)

A

non-superimposable mirror images of each other, and are said to be chiral

26
Q

define optically active

A

it rotates plane polarised light

27
Q

define diastereoisomers

A

either member of a pair of substances that differ with respect to the configurations of their molecules

28
Q

name the four types of organic reactions

A

addition, elimination, substitution, rearrangement

29
Q

what are the two types of bond formation

A

homolytic (symmetrical) and heterolytic (unsymmetrical)

30
Q

define concerted reaction

A

a chemical reaction in which all bond breaking and making occurs in a single step

31
Q

define electrophile

A

electron pair acceptor

32
Q

define nucleophile

A

electron pair donator

33
Q

describe the reaction of hydrochloric acid with ethene

A

the alkene behaves as a nucleophile and the proton from HCl behaves as an electrophile. The pi bond on the alkene breaks and the two electrons form a new bond with the proton. A carbocation is formed, which then behaves as an electrophile for the Cl-, forming a bond

34
Q
A