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LAB ACTIVITY 3 Edited 2
LAB ACTIVITY 3 Edited 2
LAB ACTIVITY 3 Edited 2
3 Structure of Hydrocarbons
INTRODUCTION
Hydrocarbon is any of a class of organic chemicals made up of only the elements carbon (C) and
hydrogen (H). The carbon atoms join together to form the framework of the compound, and the
hydrogen atoms attach to them in many different configurations. While this classification of
hydrocarbons helps to link properties to structural characteristics, it does not require that every
substance be placed in a single category. Indeed, structural units that belong to two or more
hydrocarbon families are frequently found in a molecule. For instance, a molecule with a benzene ring
and a carbon-carbon triple bond would have some properties that are typical of arenes and others that
are typical of alkynes.
Hydrocarbons were categorized by chemists in the nineteenth century as either aromatic or
aliphatic based on their sources and properties. Hydrocarbons produced through the chemical
decomposition of fats or oils were referred to as aliphatic (from the Greek aleiphar, "fat"). Aromatic
hydrocarbons were a group of related substances made by chemically breaking down some plant
extracts with pleasant odors. Modern terminology keeps the terms aliphatic and aromatic, but the
compounds they describe are differentiated based on their structure rather than their origin.
I. OBJECTIVES
l. OBJECTIVES
II. MATERIALS
Materials Actual Photo
Barbecue sticks
Protractor
Styrofoam balls
Illustration board
Poster Paints
Glue Gun
Glue Stick
III. PROCEDURE
Aside from filling out the table, construct the structures of the highlighted HCs and apply the
necessary angles.
A. Structure of Alkanes
Alkane Lewis structure Bond angle
methane, CH4 109.5°
2-methypropane, 109.5°
CH3CH3CHCH3
B. Structure of Alkenes
Alkene Lewis structure Bond angle
ethene, H2C=CH2 120°
C. Structure of Alkynes
Alkyne Lewis structure Bond angle
ethyne, HC≡CH 180°
1- butyne,HC≡ 180°
CCH2CH3
D. Structure of Arenes
Lewis structure Bond angle
Benzene 120°
Toluene 120°
E. Structure of Cycloalkanes
Lewis structure
Cyclopentane – envelope and half-chair
V. DISCUSSION OF RESULTS
We must to illustrate its Lawis structure to be a guide to assemble the carbon and
hydrogen ,the hydrocarbon is any of a class of organic chemicals made up of only the elements
carbon (C) and hydrogen (H) while the single bond is a chemical bond between two atoms
involving two valence electron and by using this it is simple to construct any structure precisely.
VI. CONCLUSION
In this activity, we made Lewis structures for each of the Alkanes, Alkenes, Alkynes and
Arenes listed in the table. While we are making the structures, we are also finding out the bond
angles of each one.
VII. QUESTIONS
The main difference between aliphatic and aromatic hydrocarbons is that aliphatic
hydrocarbons have a high carbon-to-hydrogen ratio whereas aromatic hydrocarbons have
a low carbon-to-hydrogen ratio.
2. How are aliphatic hydrocarbons different from aromatic hydrocarbons?
The main difference between aliphatic and aromatic hydrocarbons is that aliphatic
hydrocarbons have a high carbon-to-hydrogen ratio whereas aromatic hydrocarbons have
a low carbon-to-hydrogen ratio.
3. How are cyclic hydrocarbons different from aromatic hydrocarbons?
A cyclic hydrocarbon is a hydrocarbon in which the carbon chain joins to itself in a
ring. A cycloalkane is a cyclic hydrocarbon in which all of the carbon-carbon bonds are
single bonds. Like other alkanes, cycloalkanes are saturated compound while aromatic
hydrocarbons are cyclic, planar compounds that resemble benzene in electronic
configuration and chemical behavior.
4. What is hybridization and identify the type of hybrid orbitals in alkanes, alkenes, alkynes,
cycloalkanes?
Each of the carbon atoms in an alkane has sp3 hybrid orbitals and is bonded to four
other atoms, each of whickly is either carbon or hydrogen. Alkane bond are in state of
sp3 hybridzation. Alkene bond are in state of sp2 hybridzation, in sp2 hybridization ones
orbital combines with two p orbitals to form three equivalent sp2 hybrid orbitals. Alkynes
bond are in state of sp hybridization, in sp hybridization one s orbitals combines with one
p orbital to form two equivalent sp hybrid orbitals. Cycloalkane are sp3 hybridized, the
hybridization in which one s-orbital and three p-orbitals are mixed to form four identical
hybrid orbitals is called sp3 hybridization.
CHEM 109 (Organic)
BSC- 2103
Group 2
Submitted to:
Edward F. Gonzales
Instructor
September 30,2022