CHEM final exam (grade 12)

0.0(0)
studied byStudied by 0 people
call kaiCall Kai
learnLearn
examPractice Test
spaced repetitionSpaced Repetition
heart puzzleMatch
flashcardsFlashcards
GameKnowt Play
Card Sorting

1/63

encourage image

There's no tags or description

Looks like no tags are added yet.

Last updated 5:31 AM on 6/17/25
Name
Mastery
Learn
Test
Matching
Spaced
Call with Kai

No analytics yet

Send a link to your students to track their progress

64 Terms

1
New cards

SOme rules of naming compounds

-fINd the longest chain

-name so you have the smallest numbers possible

- //: -#- enes

- ///: - # - ynes

  • alphabetical order (chaines)

2
New cards

naming format

knowt flashcard image
3
New cards
<p>cycloalkane</p>

cycloalkane

__ ,__- ____ylcyclo____

ex. 1-methyl-3-ethylcyclohexane

4
New cards
<p>cycloalkane</p>

cycloalkane

_ ,__- _cyclo____yl ______

ex. 1-cyclobutylpentane

<p><strong>_ ,</strong>__- _cyclo____yl ______</p><p>ex. 1-cyclobutylpentane</p>
5
New cards
<p>Aromatic hydrocarbon </p>

Aromatic hydrocarbon

_ ,__- ____ylbenzene

ex. 1-ethyl-3-methylbenze

6
New cards
<p>Aromatic hydrocarbon </p>

Aromatic hydrocarbon

_ ,__- _phenyl______

ex. 1-phenylpentane

7
New cards
<p>haloalkanes</p>

haloalkanes

__- _(F/Cl/Br/I)_____

  • fluoro, chloro, bromo, iodo

ex. 3-bromo-6-chlorooctane

8
New cards
term image

Alcohol (R-OH)

__- ____yl___- (c #0)- ol

ex. butan-2-ol

9
New cards
term image

Carboxylic acid

__- ___yl_____oic acid

ex. pentanoic acid

10
New cards
term image

Aldehyde

__- ____yl___al

  • O= determines the root chain

  • alwayd on the end so no numbers needed (At end)

ex. 2-methylbutanal

11
New cards
term image

Ketone

  • O= determines root chain

  • O is prioritized

  • drop the e at the end

__- ____yl___- (c #0)- one

ex. propanone

12
New cards
term image

Ester

  • root chain is determined by O=

short chain-_-____yl rootcahin oate

ex. ethyl-3-methylbutanoate

13
New cards
term image

Ether

(the # C that O is attached too on the longest chain) short chain oxy-_-____yl root chain

  • O is prioritized

ex. 1-methoxy-4-methylpentane

14
New cards
term image

Amine

N-_chain_-N- chain root chain - (the # C that N is attached too on the longest chain) - amide

ex. N-ethyl-N-methylbutanamine

15
New cards
term image

Amide

N-_____-__-______________________amide

ex. N,N-methylbutanamide

16
New cards

what happens in an addition reaction?

the double / triple bonds break

Alkenes

C=C + X-Y —> X-C-C-Y

Alkynes

  • if limited ≡ —> =

  • if excess ≡ —> -

Multiple Products

2 possible products

C=C-C + X-Y —> CX-CY-C or CY-CX-C

17
New cards

Markovmikov’s Rule

Unsymetrical:

Major (H is added to the carbon with the most H)

Minor (H is added to the carbon with the less H)

18
New cards

What happens in an elimination reaction?

forms double bonds

CH2X-CH2Y —> CH2=CH2 +X-Y

  • Alcochols perform with strong acids (H2SO4)

  • Haloalkanes preform under strong bases (NaOCH2CH3)

19
New cards

Major/Minor law / anti markovnikov rule

is the double bond can be formed in more then one place, then the H will be removed from the carbon with the most carbons attached to it (major)

<p>is the double bond can be formed in more then one place, then the H will be removed from the carbon with the most carbons attached to it (major)</p>
20
New cards

what happens in a substituons reaction?

they swap

<p>they swap </p>
21
New cards

what happens in a condensation reaction?

2 molecules combine and form larger molecule + H2O

<p>2 molecules combine and form larger molecule + H2O</p>
22
New cards

what happens in an estérification reaction

condensation reaction between carboxylique acid and alcohol

<p>condensation reaction between carboxylique acid and alcohol </p>
23
New cards

what happens in a hydrolysis reaction

ester + water —> carboxyic acid + alcohol

<p>ester + water —&gt; carboxyic acid + alcohol </p>
24
New cards

what happens in an oxidation reaction?

gains O lose H (alcohol + [O])

1^o. -OH + excess [O] —> aldehyde —> carboxylic acid

2^o. -OH + excess [O] —> ketone

3^o. -OH + [O] —> N.R.

<p>gains O lose H (alcohol + [O])</p><p>1^o. -OH + excess [O] —&gt; aldehyde —&gt; carboxylic acid  </p><p>2^o. -OH + excess [O] —&gt; ketone</p><p>3^o. -OH + [O] —&gt; N.R.</p>
25
New cards

what happens in a reduction reaction ?

  • gains [H] lose O (K,A, or CA + [H] makes -OH)

<ul><li><p>gains [H] lose O (K,A, or CA + [H] makes -OH)</p></li></ul>
26
New cards

what happens in combustion reactions?

  • complete: hydrocarbon + O2 —> CO2 + H2O + energy

  • incomplete: hydrocarbon + O2 (insufficient) —> C + CO + CO2 + H2O + energy

27
New cards

what happens in a polymer addition reaction?

reduces carbons double bond and makes a pattern

28
New cards

what happens in a polymer condensation reaction?

takes an OH off of one and H from the other to make H2O and a pattern

29
New cards

john dalton

described that matter is made up of small indestructible and indivisible shares (atoms)

30
New cards

JJ Thomson

used glass discharging tubes with trace amounts of gas and passed an electric current though it. rays appeared, which curved with a magnet showing they were negatively charged. (found out there was a + and - charge in a atom) (plum pudding boy)

31
New cards

Ernest Rutherford

Fired alpha particles at a thin sheet of gold surrounded by zinc sulfuric coated screen that light up when hit with alpha particles. some particles had a large particle deflection, meaning most of the mass and all positive charges surround a very dense center (nucleus) while electrons orbit around it.

(nuclear model)

32
New cards

what happens to element when they are energized

they give off specific wavelength of light

33
New cards

Niels Bohr

  • electrons orbit like planetary orbits

  • the force that holds electrons together is electrostatic force betweent and - charges on electrons

  • electrons only exist in energy levels

  • electrons can jump between energy levels by absorbing or emitting energy

  • planetary model (didn't explain larger atoms)

34
New cards

what are the quantum numbers and do they describe

  • n, 1, ml,: describes the distribution of electrons in atoms

  • n: energy levels and size

  • I : shape

  • ml: 3D orientation

  • ms: behaviour of specific electron

35
New cards

charaistics of n

• tells you the energy level and size of orbital

* (all orbitals with the same value of n are in the same shell/energy level)

  • greater value of n means greater probability of finding an electron farther from the nucleus

  • electrons can jumps to different levels of n (absorlos energy when it goes up, and releases it when goes down)

36
New cards

stuff about I

  • shape of orbital

  • also callEd sublevels or subshells

  • 1 = n-1 (possible values)

  • 0=5, 1=p, 2=d, 3=f

37
New cards

stud about ml

• Choose from -I to +l, indicating the 3D orientation of orbitals. The total number of orbitals for an energy level n is n²

38
New cards

pauli exclusion principle

• no 2 electrons around an atom can have the same 4 Q numbers (electrons in the same orbital have same 3 Q's but different spins)

39
New cards

Aufbau principle

electrons occupied the lowest energy orbitals first

40
New cards

hunds rule

the lowest energy level of a atom has the max amount of unpaired allowed

41
New cards

ionic bonds

  • metal + non-metal

  • metals lose there electrons and non metals gain

  • opposites attract and form a crystal lattice

42
New cards

covalent bonds

non metal + no metal

43
New cards

metallic bonds

  • metal + metal

  • since 2 metals have a valance shell that are less then 8, they create a sea of valence electrons

  • low EN

  • valence electrons move freely from one atom to the next

44
New cards

Valance bond theory

a covalent bond (share electrons) forms when the orbitals of 2 atoms overlap and share a common region in space where a pair of electrons are

45
New cards

Hybrid orbitals

formed by the combination of 2 or more orbitals in the valence shell of an atom.

46
New cards

PI bonds

covalent bonds formed by the overlap of P orbitals/formed from double bonds

47
New cards

VSEPR Theroy

  • valance shall electron pair repulse theory

  • electron groups around an atom are positioned as far away from each other

(electron groups are lone pairs, single, double and triple bonds)

48
New cards

first law of thermodynamics

energy cannot be created or destroyed only transferred

49
New cards

second law of thermodynamics

when objects are in thermal contact that heat will be transferred from the object will the higher temperature to the object with the lower infill both objects have the same temperature and reach thermal equilibrium

50
New cards

what are the 6 Factors Affecting Reaction Rate

  • Nature of the reactants

  • Concentration of solution

  • Temperature

  • Pressure of Gases

  • Surface area of the particles of a solid

  • Presence of a catalys

51
New cards

Keq’s relation to one

Keq >1 favoris products

Keq < favours reactants

52
New cards

change in concentration (product up and down)

product more reactents formed

product more product formed

53
New cards

change in pressure

pressure more/shift towards side with fewer particles

pressure shift to side with more particles

54
New cards

Temperature increase

Toward endothermic reaction → Endothermic forward reaction Keq Increases

55
New cards

Temperature decrease

Toward exothermic reaction → exo increase keq

56
New cards

Properties of Ionic compounds

Crystal Lattices

High MP and BP (In the range of metals [some above some below])

Soluble (positive and negitve meds of ploles)

Hard and Brittle (With enough force, the ions can “shift” and now repel.)

Conductive if dissolved in water (so ions to move and conduct electricity)

57
New cards

Intramolecular bonds

exist within a molecule.

58
New cards

Intermolecular forces

Dipole-Dipole

Dipole induced dipole

Dispersion forces aka Van der Waals forces

59
New cards

Dipole-Dipole

When a covalent molecule is polar it has a permanent dipole

These dipoles can line up and cause attraction to each other

60
New cards

Induced Dipole

Bringing a polar molecule near a non-polar one can induced a dipole.

The molecules than have a small attraction to each other.

61
New cards

Dispersion Forces

Attractive forces between non-polar molecules.

Electrons orbit nuclei and cause brief momentary (but ongoing) moments of slight polarity.

Temporary dipole.

Very weak, but when many occur at the same time, can have a significant effect.

62
New cards

structure isomère

same formula diff shape

63
New cards

distereomer

same formula different properties

64
New cards

anti imores

mirror images