Chemistry Investigatory Project
Chemistry Investigatory Project
Chemistry Investigatory Project
●WHAT IS ALCOHOL?
In chemistry, an alcohol is a type of organic compound that carries at least
one hydroxyl (−OH) functional group bound to a saturated carbon atom.
The term alcohol originally referred to the primary alcohol ethanol (ethyl
alcohol), which is used as a drug and is the main alcohol present in
alcoholic drinks. An important class of alcohols, of which methanol and
ethanol are the simplest examples, includes all compounds which conform
to the general formula CnH2n+1OH. Simple mono alcohols that are the
subject of this article include primary (RCH2OH), secondary (R2CHOH)
and tertiary (R3COH) alcohols.
Alcohols are polar, since they have oxygen-hydrogen bonds, which allow
alcohol molecules to attract each other through hydrogen bonds. Since
oxygen atoms are much more electronegative than hydrogen atoms, the
oxygen-hydrogen bond is especially polar. The partially-negatively charged
oxygen atom on one alcohol molecule is strongly attracted to the partially
positively charged hydrogen atom on another alcohol molecule; this strong
attraction results in much stronger intermolecular forces between alcohol
molecules than there are between nonpolar alkanes of the same molar
mass. low-molecular weight alcohols such as methanol and ethanol are
miscible with water, and solubility decreases as the number of carbons in
the alcohol increases.
REACTIONS
➡️Temporary effects you might notice while drinking alcohol (or shortly
after) can include:
●WHAT IS ESTER?
The word ester was coined in 1848 by a German chemist Leopold
Gmelin, probably as a contraction of the German Essigäther, "acetic
ether".Esters are chemical compounds derived by reacting an oxoacid with
a hydroxyl compound such as an alcohol or phenol. Esters are ubiquitous.
Most naturally occurring fats and oils are the fatty acid esters of glycerol.
Esters with low molecular weight are commonly used as fragrances and
found in essential oils and pheromones. Their flexibility and low polarity is
manifested in their physical properties; they tend to be less rigid (lower
melting point) and more volatile (lower boiling point) than the
corresponding amides. Esters have the general formula R–COO–R′, which is
similar to that of the organic acid, but the H of the –COOH has been replaced by
a hydrocarbon group. The ending of the name of an ester is ate, such as in ethyl
acetate
REACTIONS
●PROPERTIES OF ESTER
● The name of an ester is derived from its carboxylic acid that takes
part in the esterification reaction.
● They have a pleasant smell.
● They have a wide application in the perfume and food industries.
● Esters are organic compounds found in oils and fats.
●USES OF ESTERS
● Esters that have fragrance are used in perfumes, food flavorings, and
cosmetics.
● Used as an organic solvent.
● Nitroglycerin is known and famous for its explosive properties.
● In the manufacturing of surfactants like detergents and soaps.
● Natural occurring esters are present in pheromones
● The backbone of DNA molecules is formed by phospho esters.
● Polyesters are used in the production of plastics
●EXAMPLES OF ESTERS
REACTIONS
●ESTERIFICATION
●ESTERIFICATION METHODS
●REMOVAL OF ALCOHOL
THROUGH ESTERIFICATION
ABSTRACT
INTRODUCTION
II THEORY:
II.1 REACTIONS:
Hydroxide
II.2 CALCULATIONS:
REACTIONS
using,
M1V1 = M2V2
(1000 x 0.03)/0.67
= 44ml
=1.48g
III. PROCEDURE
accuracy )
IV. OBSERVATIONS
1. Alcohol reacts with acetate ions present in the solution to form ester ,
ethyl acetate.
ii. Formation of MnO2- ions gives the brown color and suggests reduction
of alcohol.
REACTIONS
V. CONCLUSION
1. Alcohol can be harmful to the human body as it can cause heavy damage
to the liver like liver cirrhosis. Short term effects on the brain include
dizziness, drowsiness, loss of concentration, and mood swings. Long term
effects
4. Usually our liver takes 10-12 hours to reduce alcohol but this might prove
to be a faster solution.