Biochem Prelab 1

Serrano, Kimberly Anne M.
1N2
NUTRITIONAL BIOCHEMISTRY LABORATORY

ND 732
PRE-LAB # 2
1. What functional groups can we find in the structure of carbohydrates? Write down their
structure.
As stated in Socratic, Carbohydrates can contain hydroxyl (alcohol) groups, ethers, aldehydes
and/or ketones. Carbohydrates are chains (or polymers) of basic sugar molecules such as
glucose, fructose and galactose. In order to see which functional groups are present in
carbohydrates, we must look at the functional groups present in the more basic building blocks.
Saccharides – and by extension carbohydrates – are composed of only three atoms: carbon,
hydrogen and oxygen. The structure for one of the most common saccharides, glucose. Here we
can identify multiple hydroxyl (alcohol) functional groups and one aldehyde functional group.
Bond is bridged by two carbons instead of one carbon and one hydrogen, it is a ketone functional
group Lastly, we must consider functional groups that arise through the linking of saccharides.
Below is the structure of a disaccharide carbohydrate consisting of glucose and fructose. Notice
that here both glucose and fructose are drawn in their cyclic ring form. The two saccharides are
linked through an oxygen atom. This link is called a glycosidic bond. Since the glycosidic bond
has the form, it is an ether.
2. What are the major classifications of carbohydrates?

The major classifications of carbohydrates are simple carbohydrates and complex carbohydrates.
Simple carbohydrates are also called as monosaccharides and disaccharides while the complex
carbohydrates are polysaccharides.
3. What are the general tests in identifying the presence of carbohydrates? Explain their
principles.
TESTS ON CARBOHYDRATES:
1) Molisch’s Test: Molisch’s Test is a sensitive chemical test for all carbohydrates, and some
compounds containing carbohydrates in a combined form, based on the dehydration of the
carbohydrate by sulfuric acid to produce an aldehyde (either furfural or a derivative), which then
condenses with the phenolic structure resulting in a red or purple-colored compound.
2) Carbohydrates as Reducing Sugars: A reducing sugar is any sugar that, in a solution, has an
aldehyde or a ketone group. The enolization of sugars under alkaline conditions is an important
consideration in reduction tests. The ability of a sugar to reduce alkaline test reagents depends on
the availability of an aldehyde or keto group for reduction reactions. A number of sugars
especially disaccharides or polysaccharides have glycosidic linkages which involve bonding a
carbohydrate (sugar) molecule to another one, and hence there is no reducing group on the sugar;
like in the case of sucrose, glycogen, starch and dextrin. In the case of reducing sugars, the
presence of alkali causes extensive enolization especially at high pH and temperature. This leads
to a higher susceptibility to oxidation reactions than at neutral or acidic pH. These sugars,
therefore, become potential agents capable of reducing Cu+2 to Cu+, Ag+ to Ag and so fort.
Most commonly used tests for detection of sugars are Fehling’s Test, Benedict’s Test and
Barfoed’s Test.
a) Fehling’s Test: Fehling’s Solution (deep blue colored) is used to determine the presence of
reducing sugars and aldehydes.
b) Barfoed’s Test: Barfoed’s reagent, cupric acetate in acetic acid, is slightly acidic and is
balanced so that is can only be reduced by monosaccharides but not less powerful reducing
sugars. Disaccharides may also react with this reagent, but the reaction is much slower when
compared to monosaccharides.
c) Seliwanoff’s Test: Seliwanoff’s Test distinguishes between aldose and ketose sugars. Ketoses
are distinguished from aldoses via their ketone/aldehyde functionality. If the sugar contains a
ketone group, it is a ketose and if it contains an aldehyde group, it is an aldose. This test is based
on the fact that, when heated, ketoses are more rapidly dehydrated than aldoses.
d) Bial’s Test: Bial’s Test is to determine the presence of pentoses (5C sugars). The components
of this reagent are resorcinol, HCl, and ferric chloride. In this test, the pentose is dehydrated to
form furfural and the solution turns bluish and a precipitate may form.
3) Action of Alkali on Sugars
4) The Inversion of Sucrose: Sucrose is a disaccharide, which means that it is a molecule that is
derived from two simple sugars (monosaccharides). In the case of sucrose, these simple sugars
are glucose and fructose. Inverted sugar is a mixture of glucose and fructose. It is obtained by
splitting sucrose into these two components. The splitting of sucrose is a hydrolysis reaction
which can be induced simply by heating an aqueous solution of sucrose. Acid also accelerates
the conversion of sucrose to invert.
5) Iodine Test: Iodine test is an indicator for the presence of starch. Iodine solution (iodine
dissolved in an aqueous solution of potassium iodide) reacts with starch producing a blue-black
color.

Biochem Prelab 1

Uploaded by

Copyright:

Available Formats

Biochem Prelab 1

Uploaded by

Document Information

Original Title

Copyright

Available Formats

Share this document

Share or Embed Document

Sharing Options

Did you find this document useful?

Is this content inappropriate?

Copyright:

Available Formats

Biochem Prelab 1

Uploaded by

Copyright:

Available Formats

Serrano, Kimberly Anne M.

NUTRITIONAL BIOCHEMISTRY LABORATORY

2. What are the major classifications of carbohydrates?

3) Action of Alkali on Sugars

You might also like