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KEMORG Review 1 - Introduction and Recap

Total questions: 53

Worksheet time: 29mins

Name
Class
Date
1.

(1.2) 2 atoms bond in order to _____

a)

achieve octet e- config.

b)

achieve stability

c)

increase electronegativity

d)

become more acidic or basic

2.

(1.2) Bonding that involves sharing of electrons between elements with little to no electronegativity difference

a)

ionic

b)

metallic

c)

covalent

d)

nuclear

3.

(1.2) which of the following is a MOLECULE

a)

Mg

b)

NaCl

c)

e-

d)

H2

4.

(1.2) How many covalent bonds can be formed from an atom with 5 valence electrons

a)

2

b)

3

c)

4

d)

5

5.

(1.3) Lewis structures represent the actual bonding between atoms in a compound

a)

true

b)

false

6.

(1.3) Which formal charge is most stable?

a)

-3

b)

+2

c)

1

d)

0

7.

(1.4) Ethanol (CH3CH2OH) and dimethyl ether (CH3OCH3) are ______

a)

isotopes

b)

isomers

c)

acids

d)

alkanes

8.

(1.5) Elements in 3rd row of periodic table tend to be octet exceptions, specifically

a)

incomplete octet

b)

expanded octet

c)

free radicals (odd no. of e-)

d)

even no. of e-

9.

(1.6) what differs in between resonance structures

a)

placement of atoms

b)

sum of formal charges

c)

arrangement of electrons

d)

location of sigma electrons

10.

(1.6) what actually occurs in a resonance hybrid

a)

electrons split into halves or thirds for each fractional bond

b)

electrons are expelled for more stability

c)

electrons are delocalized over 2 or more atoms

d)

double / triple bond changes location every millisecond

11.

(1.6) What does curved arrow notation show?

a)

rotation of a sigma bond

b)

transfer of energy in a rxn

c)

movement of electrons

d)

bending and stretching of a bond

12.

(1.6) what illustrates the reason why resonance is a limitation of Valence Bond Theory

a)

oxygen is made of fractional bonds

b)

all bonds in carbon dioxide have different lengths

c)

monoatomic oxygen violates the octet rule

d)

bonds in ozone are of equal strength and length

13.

(1.6) which atom does not have resonance?

a)

HSO4-

b)

O3

c)

CO3

d)

NH4

14.

Major contributors to resonance will look (more/less) similar to the actual structure

(a)  

15.

(1.7) What may affect the bond angle in a molecule

a)

VSEPR

b)

bonding electron groups

c)

non bonding electron groups

d)

electronegativity

16.

(1.7) when is electron geometry the same as molecular geometry?

a)

when there are even numbers of electrons

b)

when there are no lone pairs

c)

when halides are involved in the bond

d)

when all the electron groups are lone pairs

17.

(1.8) CH3CH2CH2CH2CH3 or CH3(CH2)3CH3 is an example of ______

a)

lewis structures

b)

aufbau structures

c)

condensed structures

d)

skeletal structures

18.

(1.8) This is an example of _____

a)

Lewis structures

b)

stick and ball structures

c)

condensed structures

d)

skeletal structures

19.

(1.9) hybridization in methane (4 e- groups)

a)

sp3

b)

sp2

c)

sp

d)

s

20.

(1.9) what must occur prior to hybridization

a)

e- promotion / excitation

b)

bond formation

c)

proton demotion

d)

valence electron collision

21.

(1.10) the pi bond in ethylene occurs on ____

a)

p orbitals

b)

s orbitals

c)

hybdridized sp2 orbitals

d)

hybridized sp3 orbitals

22.

(1.9) What is the shape of sp, sp2, sp3 hybridized orbitals

a)

dumbell

b)

asymmetric dumbell

c)

sphere

d)

boat shape

23.

(1.11) What bond does this describe?

symmetric with respect to bond axis, stronger, head on overlap across molecular plane

a)

sigma

b)

pi

c)

delta

d)

omega

24.

(1.11) why are single bonds free to rotate?

a)

single and ready to mingle~

b)

electrons are constantly providing thrust and momentum for bond to rotate

c)

pi bonds restrict rotation as they need to break and reform

d)

because of short bond length between the two bonded atoms

25.

(1.11) What is the relationship between bond length and bond strength

a)

proportional

b)

quadratic

c)

inverse

d)

unrelated

26.

(1.12) Electronegativity __________________

a)

increases down a group, decreases across a period

b)

increases across a period, decreases down a group

c)

increases down a group and across a period

d)

decreases down a group and across a period

27.

(1.12) Describes the share of electrons between 2 bonded atoms

a)

bond order

b)

bond charge

c)

bond distribution

d)

bond polarity

28.

(1.12) In a polar compound, where would there be an accumulation of electrons

a)

near the element with higher electronegativity

b)

near the element with lower electronegativity

c)

between the two atoms

d)

above and below the molecular axis

29.

(1.12) a bond with electronegativity difference of 1.7 would be

a)

Non polar covalent

b)

Polar covalent

c)

Ionic

d)

Metallic

30.

(1.13) How do you find the net dipole moment in a molecule

a)

parallelogram method

b)

adding the individual dipole moments regardless of direction

c)

subtracting the individual dipole moments regardless of direction

d)

through mass spectroscopy

31.

(1.13) BF3 has a polar bond but is not a polar molecule, why is that?

a)

fluorine creates hydrogen bonds and cancels out the polarity

b)

Boron has a unique interaction with the wave functions of the sigma bonds to remove polarity

c)

rotation of the molecule spreads out the charge across the whole molecule instead of just fluorine through centripetal force

d)

the dipole moments cancel out due to the geometry of BF3

32.

(10.2) What is the general formula for an alkane

a)

Cn H2n+2

b)

C2n+2 Hn

c)

Cn H2n

d)

C2n Hn

33.

(10.2) How do you calculate the degrees of unsaturation?

a)

(saturated number of H - unsaturated number of H) / 2

b)

(unsaturated number of H) / 2

c)

(unsaturated number of H - saturated number of H)

d)

(unsaturated number of H) x 2

34.

(10.2) A molecule has a degree of unsaturation of 7, select which of the following are possible given this information

a)

1 triple bond, 2 double bonds, 3 rings

b)

0 triple bond, 3 double bonds, 2 rings

c)

3 triple bonds, 1 double bond, 0 rings

d)

1 triple bond, 1 double bond, 2 rings

e)

2 triple bonds, 0 double bonds, 2 rings

35.

(2.1 -2.4) _________ is a proton donor

a)

BL Acid

b)

BL Base

c)

Lewis Acid

d)

Lewis Base

36.

(2.1 - 2.4, 2.8) Which definition of acids and base is the most specific

a)

Arrhenius

b)

Lewis

c)

Bronsted-Lowry

37.

(2.1 - 2.4) In an amphoteric molecule (acts as an acid or base) _______ is the acidic portion of the molecule, and _______ is the basic portion of the molecule

a)

Hydrogen, Lone pairs

b)

Lone pairs, Hydrogen

c)

Lone pairs, Lone pairs

d)

Hydrogen, Hydrogen

38.

(2.1 - 2.4) In an acid-base reaction, the proton moves _____

a)

from the base to the acid

b)

from the acid to the base

39.

(2.1 - 2.4) using a curved arrow notation, an acid and base reaction will have arrows that ___

a)

goes from lone pair of base to hydrogen in acid

b)

goes from lone pair of acid to hydrogen in base

c)

goes from bond (H-A) to the acid

d)

goes from acid to the bond (H-A)

40.

(2.1 - 2.4) a strong acid has

a)

high Pka value

b)

unwilling to lose hydrogen

c)

easily loses hydrogen

d)

low Pka value

41.

(2.1 - 2.4) organic acids tend to be (stronger/weaker) than inorganic acids

(a)  

42.

(2.5) Strong acids produce

a)

weak conjugate bases

b)

strong conjugate bases

c)

conjugate bases of varying strength

d)

conjugate acids

43.

(2.5) what is the relationship of an element's electronegativity and its acidity

a)

higher electronegativity = higher acidity

b)

lower electronegativity = higher acidity

c)

odd electronegativity = higher acidity

d)

even electronegativity = higher acidity

44.

(2.5) for Conjugate bases that are anions, (e.g. Halogens) they are more stable when

a)

larger anion

b)

smaller anion

c)

higher electronegativity

d)

lower electronegativity

45.

(2.5) Why is trifluoroethanol more acidic than regular ethanol

a)

the polar bonds exasperate the unequal distribution of e- in the CB

b)

fluorine is a halogen and makes it more acidic

c)

actually ethanol is more acidic than trifluoroethanol

d)

fluorine pulls in charge from the CB through the sigma bonds and its high electronegativity

46.

(2.5) How does resonance affect acidity (by comparing conjugate bases)

a)

increases, stronger bonds due to resonance lead to stable molecule

b)

increases, delocalization of charge stabilizes the molecule

c)

decreases, net dipole moment is intensified and can tear the molecule apart

d)

decreases, attraction to proton is stronger so formation of conjugate base becomes thermodynamically unfavorable

47.

(2.5) an anion (CB) with higher s character has lower stability

a)

true

b)

false

48.

(2.6 - 2.7) Organic bases

a)

amines

b)

CH3COOH

c)

NaOH

d)

H2SO4

49.

(2.6 - 2.7) Organic bases are characterized by

a)

strong conjugate acids

b)

weak conjugate acids

c)

net positive charge

d)

net negative charge

50.

(2.8) How do BL bases and Lewis bases differ

a)

Lewis bases specifically donate e- to protons

b)

BL bases are always organic

c)

BL bases specifically donate e- to protons

d)

Lewis bases are always organic

51.

(2.8) In acid base reactions, the Lewis Acid is

a)

electrophile

b)

nucleophile

c)

e- rich

d)

e- poor

52.

(2.8) if a Lewis base forms a bond with a Lewis acid, we call that bond a _____

a)

salt bond

b)

nucleophilic bond

c)

coordinate covalent bond

d)

bond of neutrality

53.

(2.8) using curved arrow notation, the arrow will point from the ______ to the ______

a)

acid, base

b)

base, acid

c)

central atom, peripheral atom

d)

electropositive atom, electronegative atom