Stem3 Reviewer
Stem3 Reviewer
TOPIC OUTLINE:
1. Module 3 2. Module 4
Lesson 1: Stoichiometry Lesson 1: Organic
Lesson 2: The Gases Compounds
Lesson 3: Lewis Lesson 2: Structural
Structure of Molecular Isomerism &
Compound Organic Reaction
Lesson 4: Molecular
Geometry & Polarity
1 Stoichiometry
Mole Sample Problem #1:
(mol) a unit of amount or quantity of a Determine the number of particles and mass of
substance 0.85 mol Cu.
It is the amount of substance that contains
Solution:
exactly 6.02 x10²³ atoms, molecules, or ions.
1 mol = 602 000 000 000 000 000 000 000 (a) number of particles
000 pieces/particles 6.02𝑥1023 𝑎𝑡𝑜𝑚𝑠 𝐶𝑢
= 0.85 𝑚𝑜𝑙 𝐶𝑢 𝑥
A quantity used to indicate very small species 1 𝑚𝑜𝑙 𝐶𝑢
= 5.1 𝑥 1023 𝑎𝑡𝑜𝑚𝑠 𝐶𝑢
that make up matter like atoms, ions, or (b) mass
molecules. 63.55 𝑔 𝐶𝑢
A quantifying unit 0.85 𝑚𝑜𝑙 𝐶𝑢 𝑥 = 54 𝑔 𝐶𝑢
1 𝑚𝑜𝑙 𝐶𝑢
Molar Mass 1.1 Percentage Composition
(g/mol) mass of one mole of substance It is a way to express the relative abundance
numerically equal to the atomic mass of each element in a chemical substance.
used to convert mole to mass, or mass to (percent composition by mass) percent by
mole mass of each element in a compound
o P₁V₁=P₂V₂
2 Gases o PV= constant
2.1 Pressure
Sample Problem #1:
force that the gas exerts on the container A 20.0 L gas kept in a movable piston has an initial
boundaries pressure of 1.5 atm at 25°C. if the piston is allowed
1 atm, 760 torr 760 mm Hg to expand isothermally (at constant temperature) to
101325 Pa 14.7 psi, 1.01 bar 45.0 L, what will be the resulting pressure of the gas?
▪ atm = atmosphere
▪ mm Hg = millimeter Mercury
▪ Pa = pascal Given: V₁=20.0 L; P₁=1.5 atm; V₂=45.0 L
▪ psi = pounds per square inches
Requirement: P₂= ?
Barometer
measures atmospheric pressure Equation : P₁V₁=P₂V₂
5.0 𝑎𝑡𝑚 𝑃2
Sample Problem #2: =
298.15 𝐾 305.15 𝐾
Consider a 25.0 L gas in a container initially at
25.0°C and 1 atm. If this gas is heated to 80.0°C, Answer: P₂ = 29.6 L
what will happen to its volume under constant
pressure?
Solution:
Molar Mass
H = 2 x 1.01 = 2.02 g/mol O = 2 x 16.00 = 32.00
Sample Problem #6: g/mol
Calculate the volume that will be occupied by 20.0
g carbon dioxide at 25.0 °C and 1.25 atm 𝑅𝑎𝑡𝑒 𝑟𝑎𝑡𝑖𝑜 = √
32.00 𝑔/𝑚𝑜𝑙
2.02 𝑔/𝑚𝑜𝑙
All elements in Group IA (AlkalineMetals) For example, metals may lose electrons
have the same electron-dot structure and to form positively charged cations, and
therefore each can lose one electron to form nonmetals may gain electrons to form
a +1 ion with the electron configuration of negatively charged anions.
the preceding noble gas. The resulting oppositely charged ions
attract each other, forming an ionic
bond.
ii. Covalent Bonding:
3.1.2 Lewis Structure of Molecular Atoms can share electrons to achieve a
Compounds
full outer shell. In covalent bonds,
electrons are shared between atoms,
leading to the formation of molecules.
Gilber N. Lewis 3. Stability Achieved:
1875 - 1946 Through these bonding processes, atoms
Atoms combine in order to achieve a more become part of molecules or compounds
stable electron configuration. (non- with a more stable overall electron
verbatim) configuration.
This maximum stability is attained when an This stability is achieved by reaching a state
atom is isoelectronic with a noble gas. similar to that of noble gases.
o This means that an atom achieves
Octet Rule
stability if and only if it has equal
number of electrons to the noble “Elements gain or lose electrons to attain an
gas closest to it; thus, having the electron configuration of the nearest noble gas”
same electron configuration. Remember, in combining or bonding with
o Except for He, the noble gases other atoms, only the outer electrons, the
have eight outer electrons or an valence electrons, are involved.
octet of electrons.
Breakdown of the idea:
1. Stable Electron Configuration:
Noble gases (e.g., helium, neon, argon)
have a stable electron configuration.
▪ They have a full outer electron
shell (valence shell), which makes
them relatively inert and stable. Covalent Bond
Other atoms, especially those in the is a type of chemical bond that is formed
main groups of the periodic table, aim by sharing of electrons.
to achieve a similar electron This occurs between non-metals
configuration to become more stable.
2. Chemical Bonding:
Atoms can achieve a stable electron
configuration by either gaining, losing,
or sharing electrons.
▪ There are two primary types of
chemical bonds: ionic and
covalent. The representation of the covalent compound above
i. Ionic Bonding: is called the Lewis structure.
Atoms can transfer electrons to In the Lewis structure, the shared electrons
achieve a full outer shell. that form a bond are represented by a line
or a pair of dots.
c. Ammonia, NH₃
VSEPR Theory
The chemical formula of a compound has
4.1.2 Molecular Geometry
no direct relationship with its molecule.
arrangement of the atoms surrounding the
The three-dimensional shapes of molecules central atom
can be predicted from their Lewis
counts only bond pairs in the central atom.
structures, with the model known as the
valence-shell electron pair repulsion
(VSEPR) model.
According to 4.1.3 Geometry of Simple
VSEPR model, the Compounds
electron form pairs in To determine the electron-domain
the valence shell of geometry and the molecular geometry of an
an atom. atom, the electron pairs on the central atom
These electron pairs are counted.
can either be the Tables containing the electron-domain and
bond pairs or the molecular geometries of simple molecular
lone pairs. compounds is shown below and on the
Each of these electron pairs occupies its next page.
own domain but keeps other domains as far
away as possible (electron pairs repel each
other).
➢ This repulsion creates a three-
dimensional structure of the
compound; thus, a molecular
geometry.
Octahedral (AX₆):
➢ Example: SF₆
➢ Six atoms bonded to the central atom,
forming an octahedral shape with bond
angles of 90 degrees.
Guide Questions during Practice
1. What element composes the central atom?
2. How many electron pairs are present in the
central atom?
a. This value provides the electron-
domain geometry.
From the tables, you would notice that both 3. Of the electron pairs, how many are the
the bond pairs and lone pairs, when added, bond pairs? The lone pairs?
provides the total number of electron pairs a. These values provide the
(electron domain). molecular geometry.
Linear (AX₂): Sample Problems
➢ Example: BeCl₂ Determine the electron-domain geometry and the
➢ Two atoms bonded to the central atom, molecular geometry of the following compounds:
with a bond angle of 180 degrees.
Tetrahedral (AX₄):
➢ Example: CH₄
➢ Four atoms bonded to the central atom,
creating a three-dimensional tetrahedral (2) O₃
shape with bond angles of 109.5 degrees.
4.2.1 Polarity of Chemical Bonds Other than covalent bond, another type of chemical
Covalent Bond bond is the ionic bond.
Covalent bond is a type of chemical bond Ionic bonds
that is formed by sharing of electrons in form as a result of electrostatic attraction
atoms. between oppositely charged ions.
It occurs because the atoms in a compound This type of bond occurs between a metal
have similar tendency to gain electrons. and a nonmetal.
With this, there are two subtypes of
covalent bonds – the nonpolar covalent The bond between two atoms can be a polar
bond and the polar covalent bond. covalent bond, a nonpolar covalent bond, or an
ionic bond.
Nonpolar covalent bond (or simply
nonpolar bond) To determine the nature of a bond, one
➢ forms when two atoms equally share the specific property is used.
bonding electrons.
➢ Take H2 molecule as an example. Both
atoms have equal attraction (Affinity) for This property is electronegativity.
electrons; thus, forming a nonpolar bond.
4.2.2 Electronegativity
is an atom’s ability to attract an electrons
towards itself.
Stronger electronegativity means an atom
has more tendency to gain electrons.
In chemical bonds, the electronegativity
difference between the two atoms help
determine bond polarity.
Greater difference means one of the two
atoms has a stronger affinity for electrons.
Generally, if the electronegativity
difference is:
▪ 0 – less than 0.4 = nonpolar covalent
bond
▪ 0.4 – 1.78 = polar covalent bond
▪ Greater than 1.78 = ionic bond
Example: Given the following pairs, ➢ The more electronegative atom attracts the
determine the polarity of the bond: shared electrons more strongly, creating a
Note: Electronegativity difference is an partial negative charge (δ-) on that atom
absolute value and a partial positive charge (δ+) on the
less electronegative atom.
Example: Water (H₂O) is a polar molecule.
Oxygen is more electronegative than hydrogen,
leading to a partial negative charge on oxygen
Water and oil do not mix due to their and partial positive charges on the hydrogens.
polarities.
Nonpolar Molecules
Molecular Polarity ➢ Nonpolar molecules have an even
results from the uneven partial charge distribution of electrons, resulting in no
distribution between various atoms in a significant charge separation.
compound. ➢ This occurs when there is little or no
Molecular polarity differs from bond difference in electronegativity between the
polarity atoms in a covalent bond, or when the
The polarity of a molecule affects its molecular geometry cancels out the dipole
behavior. moments.
Example: Diatomic molecules like oxygen (O₂) and
nitrogen (N ₂ ) are nonpolar because the
4.2.3 Polarity of Molecules electronegativity of the two atoms is similar, and the
A molecule is considered polar if there is a linear molecular geometry cancels out the dipole
distortion of electron cloud around a moments.
molecule. Dipole Moment:
This happens due to several reason: ➢ A dipole moment is a measure of the
the presence of alone pair on the central polarity of a molecule. It is the product of
atom, the charge (Q) and the distance of
a different element in one of its terminal separation (r) between the positive and
atoms (atom attached to the central atom), negative charges: μ = Q × r.
or a combination of any of these. ➢ The dipole moment is a vector quantity,
To determine the polarity of a molecule, and its direction points from the positive
two things are considered: to the negative charge.
▪ polarity of bond Determining Polarity:
▪ molecule shape. (1) To determine the polarity of a molecule,
you can look at its molecular geometry and
The polarity of a molecule is determined by the electronegativity of the atoms involved.
the distribution of electrons within the (2) If a molecule has polar bonds but the
molecule and the resulting charge geometry results in a symmetrical
separation. distribution of those bonds, the dipole
A molecule can be either polar or nonpolar, moments may cancel out, leading to a
and this classification depends on the nonpolar molecule.
electronegativity of the atoms and the (3) If the molecular geometry and
molecular geometry. electronegativity differences result in an
Polar Molecules unsymmetrical distribution of charge, the
➢ Polar molecules have an uneven molecule is likely polar.
distribution of electrons, leading to a
separation of charges.
➢ This charge separation arises when there is
a significant difference in electronegativity A molecule’s shape can be symmetrical or
between the atoms in a covalent bond. asymmetrical.
5 Organic Compounds
These compounds are basically made up of ➢ The general formula is CnH2n+3, where n
carbon atoms bonded mostly to hydrogen, is the number of carbon atoms.
oxygen, nitrogen, and sulfur. ➢ In naming an alkane, the suffix -ane is
However, it is important to note that all added
organic compounds have carbons, but not
all carbon-containing compounds are
organic compounds.
C Atoms, Prefix
1 meth- Alkenes
2 eth- ➢ unsaturated hydrocarbon (olefins)
3 prop-
➢ General Formula: CnH2n
4 but-
➢ Naming Rule: Carbon chain prefix + -ene
5 penta-
6 hexa- ➢ are nonpolar organic compounds
7 hepta- containing a carbon to carbon double
8 octa- bond.
9 nona-
10 deca-
➢ Suffixes in the name indicate the functional
group present in the chain.
➢ To better understand, let us begin the
discussion with the simplest class of
organic compounds – the hydrocarbons. To name a straight chain alkene with only
one double bond, number the carbon
atoms of the parent chain such that the
carbon with the double bond has the lowest
5.1 Hydrocarbons
possible number.
Hydrocarbons are organic compounds
The suffix -ene is then added in the name.
containing only two elements – carbon and
hydrogen.
All other organic compounds are derived
from hydrocarbons in which one or more
hydrogen atoms have been replaced by
other atoms or groups of atoms.
Hydrocarbons can be classified as aliphatic
hydrocarbon or aromatic hydrocarbon.
Alkynes
➢ unsaturated hydrocarbon
➢ General Formula: CnH2n-2
5.1.1 Aliphatic hydrocarbon
➢ Naming Rule: Carbon chain prefix + -yne
Aliphatic hydrocarbon can be subdivided
➢ are nonpolar organic compounds
into alkanes, alkene, alkynes, and
containing a carbon to carbon triple bond
cycloalkanes.
Alkanes
➢ saturated hydrocarbon (paraffins)
➢ General Formula: CnH2(n+2)
➢ Naming Rule: Carbon chain prefix + -ane
➢ Alkanes (also called saturated
➢ the rules in naming alkynes are the same
hydrocarbon) are the most basic type of
with those if alkenes except for the suffix
organic compound.
for alkynes is -yne.
➢ These contain only single bonds.
a. CH2═CHCH2CH3
Stability and Resonance: Discussed below are the classes under hydrocarbons:
Aromatic hydrocarbons are characterized
by a high degree of stability attributed to 5.2.1 Alkanes
resonance in the benzene ring. also called paraffins
The electrons in the double bonds of the are nonpolar compounds
benzene ring are delocalized, creating a ▪ this means that these compounds are
more stable structure. hydrophobic.
In liquid form, alkanes are commonly used as
Aromaticity: organic solvents in laboratories.
Aromatic hydrocarbons exhibit a property alkanes are utilized in general anesthetics and
known as aromaticity, which is related to as fuels.
the stability of the benzene ring.
A compound is considered aromatic if it 5.2.2 Alkenes
meets certain criteria, including having a are nonpolar organic compounds and show
planar, cyclic, and fully conjugated trends in properties similar to those of alkanes
structure. example of alkenes are ethene and propene (or
propylene).
Examples:
Examples of aromatic hydrocarbons Ethene
include benzene (C₆H₆), toluene (C₇H₈), ➢ commonly known as ethylene
and xylene (C₈H₁₀). ➢ is used in synthesizing many plasticcs and
commercially important alcohols
The primary distinction between aromatic and
aliphatic hydrocarbons lies in the presence of Propene
the benzene ring. ➢ used in manufacturing polypropene
polymer
Aromatic hydrocarbons contain benzene rings o a type of synthetic polymer
and exhibit unique stability and resonance
properties, while aliphatic hydrocarbons do 5.2.3 Alkynes
not contain benzene rings and can have a are nonpolar organic compounds and
variety of open-chain or cyclic structures. exhibit the same trends in boiling point and
physical states as alkanes and alkenes.
a good example is ethyne
5.2 Organic Compound Families Ethyne
The major families of organic compounds are ➢ the simplest and smallest alkyne
characterized by their functional groups. ➢ commonly known as acetylene
For this lesson, we will be discussing three ➢ a gaseous substance commonly burned with
organic compound families: oxygen gas in a welding torch.
▪ the hydrocarbons,
▪ the oxygen-containing compounds, Alkenes and alkynes are called unsaturated
▪ the nitrogen-containing compounds. hydrocarbon because they do not contain the
maximum number of hydrogen atoms due to
Summarized below are the classes of organic the presence on the carbon to carbon double
compounds in each family. and triple bond.
Hydrocarbon Nitrogen- Oxygen-
containing containing
Alkane Amine Alcohol Other than hydrocarbons containing just carbon and
Alkene Amide Ether hydrogen, organic compounds can exist as
Alkyne Aldehyde compounds containing oxygen and nitrogen. The
Ketone kind or the family in which an organic compound
Carboxylic Acid belong to depends on the functional group present
Ester in it.
For example,
Formaldehyde
➢ Formaldehyde is soluble in water, and a 40
percent concentration called formalin has
been used as an embalming agent and to
preserve biological specimens.
➢ Formaldehyde is also a raw material used to
Diethyl ether make plastics.
➢ commonly known as ether
➢ is the best-known ether
➢ it is extremely flammable and can Ketone
sometimes exhibit explosive properties. Ketones take their name from their parent
alkane chains. The ending -e is removed and
replaced with -one.
5.2.6 Aldehyde and Ketone The common name for ketones are simply the
Both aldehydes and ketones contain the carbonyl substituent groups listed alphabetically +
group C═O as their functional group. ketone.
Ketones are less reactive than aldehydes.
The difference between the two is the
An example of ketones are acetone
substituents on the carbonyl group.
(propanone), which is used as a solvent in paint
In aldehydes, the substituents are R and H; in
removers and nail polish removers.
ketones, the substituents are both R groups.
The general formula for aldehydes and ketones
are R–COH and R–CO–R’ respectively.
Many common odors and flavors come from
Aldehydes are named by replacing the terminal – aldehyde and ketones. Examples for aldehydes
e of the corresponding alkane name with –al. In are vanillin from vanilla bean and citral (or
ketones, the suffix –one is used. citrus?) from lemongrass
Ethyl ethanoate/acetate
➢ It is used as an artificial fruit essence and
Formic acid aroma enhancer, as an artificial flavor for
➢ Formic acid or methanoic acid are secreted ice cream, cakes and confectionary, as a
by ants when they bite producing a ‘sting’ solvent and many more.
and causing the pain.
5.2.9 Amine
Acetic acid or ethanoic acid Amines are organic compounds where an alkyl
➢ Acetic acid or ethanoic acid is the acid in group is bonded to a derivative of ammonia,
vinegar. NH3.
Stearic acid Hydrogen atoms in ammonia is replaced by
➢ Many carboxylic acids, such as stearic acid, alkyl group.
are used in soap-making. This means that the number of alkyl
substituents can be up to three.
Acetylsalicylic acid The formula for amines can be R—NH2,
➢ Organic acids are also used in preparing R2—NH, or R3—N depending on the
several drug like aspirin also known as number of alkyl substituents.
acetylsalicylic acid, a medication used to
reduce pain, fever, or inflammation.
Guide Questions during Practice There are several types of isomers and these are
1. Are there functional groups in the shown below.
structure?
2. If Step 1 is a Yes; what family does the
compound belong to?
a. Each family organic compounds has a
unique method of naming.
Skeletal isomers
➢ differ in carbon linkages found in the
“skeleton” chains.
➢ The skeleton chain or the parent chain is
the longest carbon chain.
Positional isomers
➢ only differ in the attachment of the
functional group to the parent chain.
6 Structural Isomerism and Functional isomers
Organic Reactions ➢ are two or more compounds having the
same molecular formula but different
functional groups.
6.1 Isomerism
Isomers
are different compounds that have the same
Skeletal Isomers
chemical formula.
also known as chains isomers, these isomers
In other words, these are group of atoms
arise because of the possibility of branching
with the same molecular formula but
in carbon chains.
different arrangement of atoms.
an example is butane, C4H10, which has
For example, have a C4H10 molecular formula, but two chain isomers.
have different structures. o In one of them, the carbon atoms
lie in a “straight chain” whereas in
the other the chain is branched
Sample Problems
6.2.2 Condensation
A condensation reaction is characterized by the
joining of two molecules to form a larger
molecule and the elimination of a small
molecule such as water or methanol.
The general formula of a condensation Hydrohalogenation
reaction is ➢ Hydrohalogenation involves the addition
A + B → C + water/methanol* of a hydrogen atom and a halogen atom to
an unsaturated compound (containing a
carbon-carbon double bond)
6.2.3 Addition
Addition reactions occur with unsaturated
compounds –compounds containing a carbon
to carbon double and triple bonds. Hydration
Atoms or groups of atoms are simply added to ➢ a hydration reaction involves the addition
a multiple bond without the elimination of of water (H20) to an unsaturated
atoms or other molecules producing a single compound.
compound with no atoms (from the original ➢ this is one way of preparing an alcohol
compound) removed or displaced. from the corresponding alkene.
The general equation is addition reaction is
▪ compound A + compound B →
compound C 6.2.4 Saponification
▪ Notice that C is the final product with no This is process by which triglycerides (a
A or B remaining as a residue. type of fat and most often animal fats or
Addition reactions can be any of the following: vegetable oils) are reacted with sodium or
hydrogenation, halogenation, potassium hydroxide(lye) to produce
hydrohalogenation, and hydration. glycerol and a fatty acid salt called "soap.”
When sodium hydroxide is used, a hard
soap is produced. The general formula of a
Hydrogenation saponification process is
➢ Hydrogenation involves adding hydrogen
(H2) to an alkene.
➢ During hydrogenation the double bond is
broken and more hydrogen atoms are
added to the molecule
SAPONIFICATION REACTION:
➢ Fat+Lye → Soap+Glycerol
➢ The saponification reaction breaks the oil
or fat molecule into glycerin and a sodium
or potassium salt of the long hydrocarbon
chains that have a carboxylate end
functional group.