Science: Whole Brain Learning System
Science: Whole Brain Learning System
Science: Whole Brain Learning System
SCIENCE GRADE
GENERAL CHEMISTRY 1 11
4
LEARNING QUARTER
MODULE WEEK 5
0
MODULE IN
GENERAL CHEMISTRY 1
QUARTER 4
WEEK 5
Development Team
Management Team:
Vilma D. Eda, CESO V
Arnel S. Bandiola Lourdes B. Arucan
This module helps you understand the properties and reactivities of common functional
groups. In your journey through the discussions and assigned tasks, you are expected to:
Learning Objectives:
1. identify functional groups and differentiate between the various organic compounds;
2. describe and give examples of isomers; and
3. describe some simple reactions of organic compounds; combustion of organic fuels,
addition, condensation, and saponification of fats
Directions: Read the question/statement carefully. Write the letter of the correct answer
on a separate sheet of paper.
A. 3,3-diethyl-pentanone C. 2-ethyl-propanone
B. 3-pentanal D. 3-pentanone
What’s In
What’s New
The chemical reactions that sustain life processes in living organisms involve mainly
carbon-containing compounds, usually in very large molecules with hundreds or even
thousands of carbon atoms. Aside from carbon, organic compounds also contain hydrogen,
oxygen, nitrogen and other elements.
Since there are numerous compounds of carbon, it is convenient to organize them into
groups that exhibit structural similarities. The organic compounds are related to each other by
a common feature involving a certain arrangement of atoms called functional groups.
Hydrocarbons
The simplest and most commonly encountered class of organic compounds is the
hydrocarbons, made up of carbon and hydrogen only. Hydrocarbons where all carbon atoms
are linked by single bonds are called saturated hydrocarbons while those where at least a
carbo-carbon double or triple bond is present are called unsaturated hydrocarbons.
Hydrocarbons serve as fuels, lubricants, and raw materials for the synthesis of plastics, fibers,
rubbers, solvents, explosives and other industrial chemicals.
• Alkanes. Alkanes are also called paraffins (meaning ‘low affinity’), are hydrocarbons
that contain only single bonds. The general formula is C nH2n+2, where n refers to the
numbers of carbon atoms. The simplest alkane is methane, CH 4, a major component
of natural gas which is used for home heating in cold countries.
• Alkenes. Alkenes are called olefins, which contain one or more double bonds. The
general formula is CnH2n. The simplest alkene is ethene, C2H4, a plant hormone that
plays important roles in seed germination and ripening of fruits.
• Alkynes. Alkynes contain one or more triple bonds with a general formula C nH2n-2.
The simplest alkyne is acetylene or ethyne, C2H2, a highly reactive gas used in
oxyacetylene torches.
• Aromatic Hydrocarbons. The word ‘aromatic’ referred to the aromas of these
compounds. Examples of aromatic hydrocarbons are benzene (a good solvent for fats
and paints but is toxic), naphthalene, and anthracene (used in making color designs
in fabrics). Benzene, C6H6, is the simplest aromatic hydrocarbon. It is a compound of
six carbons joined together to form a ring. There are three alternating double bonds
that undergo resonance.
Ether
Diethyl ether
Aldehyde
Ethanal
(acetaldehyde)
Ketone
Propanone
(acetone)
Carboxylic
Acid Ethanoic acid
(acetic acid)
Ester Ethylacetate
(Ethyl
Ethanoate)
Amine
Ethylamine
Amide
Ethanamide
(acetamide)
Halide
Chloromethane
(Methyl
chloride)
• Alcohols. Alcohols contain the hydroxyl (OH) as the functional group and are
considered derivatives of water. Simple alcohols are named by changing the last letter
in the name of the corresponding hydrocarbon to -ol. When needed, the location of the
OH group is indicated by numerical prefix that indicates the number pf the C atom
bearing the OG group. For example,
1,2,3-propanetriol or glycerol
• Ethers. Ethers are compounds in which two hydrocarbon groups that can be aliphatic or
aromatic are attached to one oxygen atom. In naming ethers, the word ether is always
added to the names of the two alkyl groups attached to the oxygen. For example:
• Carboxylic Acid. Carboxylic acids contain the carboxyl functional group written as -
COOH, a combination of a carbonyl and hydroxyl group. The names for carboxylic acid
always end with -ic acid like ethanoic acid. Carboxylic acids are weak acids that are
widely distributed in nature and are commonly used in consumer products. It is
important in the production of polymers used to synthesize fibers, films and paints. For
example:
• Esters. An ester is formed when a carboxylic acid and an alcohol react, with water as
a byproduct. Esters are compounds in which an alkyl or aromatic group substitutes
for the hydrogen atom of the carboxyl group of carboxylic acid. Many esters are
volatile liquids with naturally pleasant odors. Some are found in fruits and are
responsible for their characteristic sweet odors. Esters are named by using the first
group from which the alcohol is derived and then the group from which the carboxylic
acid s derived; then the suffix -ate is added. For example:
One reason for the occurrence of a great number of organic compounds is the existence
of two or more different organic compounds having the same molecular formula. This is known
as isomerism.
Isomers are compounds with the same molecular formula but with different structural
formula. A compound can have one molecular formula but with different structural formulas.
For example, C5H12.
What’s More
Directions: Name and classify the following compounds based on the functional groups in
each of the following structures. (10 points)
OH
1. CH3CH2CH2CHCH2CH3
2. CH3CH2CH2OCH2CH2CH3
3. H2NCCH3
4. CH3C-O- CH2CH2CH3
5. CH3CCH2CH3
Directions: Write or draw the structural formula of each of the following compounds. (10
points)
1. 3-methyl-2-butanol
2. 2,2-dimethylhexanal
3. dipropyl ether
Directions: Read the question/statement carefully. Write the letter of the correct answer
on a separate sheet of paper.
3. The compound formed when one or more hydrocarbon chains or aromatic rings replace
the hydrogen of ammonia is called a/an ________.
A. alcohol C. amide
B. amine D. ethers
4. An aldehyde contains what functional group that is located at the end of a carbon chain?
A. carbonyl group C. hydroxyl group
B. carboxyl group D. ammonia group
9. Compounds with the same molecular formula but with different structural formula is
called ____________.
A. compounds C. isomers
B. isotopes D. functional groups
10. What is the IUPAC name for the compound shown below?
A. 2-methyl-4-pentanone C. 2-methyl-pantanol
B. 4-methyl-2-pentanone D. methyl-2-methyl-propanoic acid
References
Davis, Raymond E., et.al, Modern Chemistry. Austin, Texas: Holt, Rinehart and Winston.
2002.
Bayquen, Aristea V., et.al, Exploring Life Through Science Series Senior High School General
Chemistry 2. Quezon City: Phoenix Publishing House, Inc. 2016.
Barrameda, Ma. Corazon, et.al, Teaching Guide for Senior High School General Chemistry 2.
Quezon City: EC-TEC Commercial. 2016.
Padolina, Ma. Cristina D., et.al, Conceptual and Functional Chemistry-Modular Approach.
Quezon City: Vibal Publishing House, Inc. 2010.
Ilao, Luciana V., et.al, General Chemistry 2. Manila: Rex Book Store. 2017
Petrucci, Harwood, Herring, and Madura. General Chemistry: Principles and Modern
Applications. 9th ed. Upper Saddle River, New Jersey: Pearson Education, 2007.
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