Chapter 2- Water, Carbohydrates and lipids Flashcards
Abundance of carbon
In a carbon atom, the four electrons in its outer shell repel each other and thus push away to shape the atom into a tetrahedron.
Carbon’s four such bond sites form covalent bonds that are stable and strong enough larger molecules.
Carbohydrates
Also known as saccharides or sugars.
Acts as an energy source and store.
Contains carbon, hydrogen and oxygen.
Appears in the ratio, Cx(H2O)x
A single unit is called monosaccharide. Ex: glucose, fructose and ribose.
When two monosaccharides join, they form disaccharide. Ex: lactose, sucrose
When two or more monosaccharides are linked they form a polymer, polysaccharide. Ex: Glycogen, cellulose and starch. These are large carbs.
What is Glucose? What is Alpha and beta?
The biochemical energy in its bonds are released during cellular respiration.
Is a monosaccharide and has a hexose structure (has six carbons)
Other hexose monosaccharides include fructose and galactose.
Has a formula of C6H12O6
In diagrams, the carbons are numbered clockwise beginning with the carbon to the right of the oxygen atom within the ring.
Two types- alpha and beta
The position of OH differs in these structures.
Alpha and beta glucose molecules are isomers.
Is glucose soluble in water?
Glucose molecules are polar and soluble in water
The lone pair of oxygen in the water molecule and the OH in the glucose molecule form hydrogen intermolecular interactions.
Due to this the glucose is dissolved in the cytosol of the cell.
It is the main respiratory substrate resulting in energy being released
Can be broken down into smaller and simpler molecules such as CO2 and H2O.
What happens in a condensation reaction between alpha glucose molecules?
Two hydroxyl groups interact with each other when two alpha molecules are side by side.
When this happens, bonds are broken and new bonds reforms in different places producing a 1-4 glycosidic bond and a water molecule.
It is called 1-4 glycosidic bond because carbon-1 from one glucose and carbon-4 from another glucose molecule bond.
Most organisms can only break down polymers of alpha glucose, they do not have the necessary enzymes to break down polymers of beta glucose.
Polarity of a water molecule
In a water molecule, the oxygen atoms are bigger and also more electronegative than hydrogen atoms.
It attracts the electrons in the outmost shells of the adjacent hydrogen atoms. This is why it has a higher share of electrons than hydrogen atoms. It leaves some regions positive, and others negative. (See appendix)
Hydrogen bonds in a water molecule
Hydrogen bonds are relatively weak intermolecular interactions which break and reform between constantly moving water.
When a water molecule forms bonds, the negative and positive regions interact with each other.
Boiling point of water
Has an unusually high boiling point due to hydrogen bonds in a water molecule
Water is a liquid at room temperature
Requires a lot of energy to increase the temperature of water and convert its state to a gas.
Density of water
At solid state, its density is lower.
This is because the hydrogen bonds form slightly further apart
What is the opposite of condensation reaction?
Opposite of condensation reaction is hydrolysis.
Hydrolysis breaks down all Non-reducing sugars to reducing sugars.
Non- Reducing sugars include disaccharides (except maltose)and polysaccharides.
Reducing sugars are monosaccharides- ex: glucose, fructose, ribose etc
Two ways we can carry out a hydrolysis reaction, is by boiling a reducing sugar along with dilute acid and also by using enzymes.
It is an enzyme controlled reaction.
Examples of monosaccharides (hexose and pentose)
Glucose is a hexose
Source of energy as easily hydrolysed; transported in the blood of animals.
Fructose is a hexose too
Isomerase converts fructose to glucose and back.
Ribose and deoxyribose are pentose
Ribose are part of all types of RNA molecules and ATP molecules, so it is an important part of protein synthesis.
Deoxyribose is a part of DNA for inherited information
Both of these are important in forming nucleic acids (acids formed by nucleotides)
Triose sugars are important for respiration and photosynthesis.
Only monosaccharides can provide energy
Examples of disaccharides
These are small and soluble
Maltose-> glucose + glucose
This is formed when amylase breaks down starch by a hydrolysis reaction.
Sucrose-> glucose + fructose
Lactose-> glucose + galactose
Fructose is sweeter than glucose and this is sweeter than galactose
Examples of polysaccharides
These are large, complex, insoluble and stable molecules
Starch- this form of saccharide is found in plants
Glycogen- this form of saccharide is found in animals
Cellulose- structural and strong molecule which forms the cell wall in plants and algae
Starch and glycogen
Many alpha glucose molecules can be joined by glycosidic bonds to form two slightly different polysaccharides, collectively known as starch.
Glucose is formed through photosynthesis and is stored as starch in amyloplasts ( a type of plastid) in plant organs.
In animals, glucose that is not needed immediately, is stored as glycogen in muscle and liver cells.
What is a plastid
Specialised membrane-bound organelles found in plant cells, for example chloroplasts and amyloplasts.
These store starch grains.
Amylose
Is made by alpha glucose molecules joined only by 1-4 glycosidic bonds.
This long of glucose twists to form a helix due to the angle of the bond. This is reinforced by hydrogen bonding within the molecule.
This makes it less soluble.
Amylopectin
Consists of 1-4 glycosidic bond along with 1-6 glycosidic bond
It is a long branched chain with short side arms of glucose units attached to the main chain of 1-4 glycosidic bonds. These short arms are the 1-6 glycosidic bonds.
This is makes it more compact than amylose.
Amylose and the iodine test
Iodine gets trapped in the coiled structure of amylose resulting in the solution becoming blue-black.
Why is the structure of starch ideal for storage
Compact and stable due to coiling and folding
Individual bonds are weak but multiple are stable
Is insoluble; therefore does not affect water potential and osmotic properties.
Can be easily broken down by enzymes into glucose when needed.
Cellulose
Formed by beta glucose molecules
In a beta molecule, the hydroxyl group of carbon-4 is at the bottom while the hydroxyl group of carbon-1 is at the top.
These groups cannot react since they are too far.
The only way that beta glucose molecules can join together and form a polymer is if the hydroxyl group in the second beta glucose molecule is turned upside down.
When a polysaccharide is formed from glucose in this way it is unable to coil or form branches
Which is why it only forms straight chain molecules
How is a fibre made?
Cellulose chains have many OH groups on the outside which allows hydrogen bonds to form between the cellulose chains. This form microfibrils. There are cross links between cellulose chain in a microfibril.
These microfibrils join together through hydrogen bonds forming macro fibrils
These then form fibres by hydrogen bond cross links.
Fibres are strong and insoluble. These are used to make cell walls.
It is hard to break down the monomers that form the ‘fibre’ or ‘roughage’ necessary for a healthy digestive system.
Differences between Glycogen and Amylopectin
They both are branched chains due to the 1-6 glycosidic bonds joining the main chain of 1-4 glycosidic bonds
However, the glycogen chain tend to be shorter and so the molecules are very compact.
There are 1-6 glycosidic bonds every 24 to 30 1-4 glycosidic bonds in an amylopectin
There are 1-6 glycosidic bonds every 8 to 12 1-4 glycosidic bond in a glycogen.
Glycogen is stored as granules in muscle and liver cells.
How quickly is energy available in reducing and non-reducing sugars
reducing sugars release energy easily
Polysaccharides need to be broken down in order to release energy
Other examples of polysaccharides
Chitin- the cell wall of fungi
Peptidoglycan or meurein- the cell wall of prokaryotic cells