[Unit 1.2/3/4] | Carbohydrates Flashcards

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1
Q

List 3 Monosaccharides

A

“FGG”: Fructose, Glucose, Galactose

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2
Q

List 3 Disaccharides

A

“SLM”: Sucrose, Lactose, Maltose

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3
Q

List 4 Polysaccharides

A

“CAGS”: Celluose, Amylopectin, Glycogen, Starch

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4
Q

What does -saccharide classify?

A

Classifies carbohydrates containing sugars

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5
Q

How many monosaccharides form a disaccharide and how many form a polysaccharide?

A

2 form a disaccharide
3+ form a polysaccharide

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6
Q

On a diagram of an alpha/beta glucose molecule is carbon 1 found on the left or right of the oxygen atom?

A

Right.
Carbon 1-6 can be found clockwise from the oxygen atom.

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7
Q

What is the difference between an alpha and a beta glucose molecule?

A

Bonded to the carbon 1 atom, the alpha glucose molecule will have a hydrogen atom above and a hydroxyl group below.
The beta glucose molecule has the opposite: the hydroxyl group is above and the hydrogen atom is below.

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8
Q

Describe the colour change observed within a solution containing a reducing sugar when Benedict’s Solution & 70°C of heat are added.

A

Brick Red

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9
Q

List the products of the condensation of Glucose + Glucose.

A

“GluGluM”: Maltose + Water

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10
Q

List the products of the condensation of Fructose + Glucose.

A

“FruGluS”: Sucrose + Water

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11
Q

List the products of the condensation of Glucose + Galactose.

A

“GluGaL”: Lactose + Water

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12
Q

Explain what occurs between the C1 and C4 of 2 glucose molecules to form maltose.

A

A condensation reactions occurs and from the 2 hydroxyl groups, 2 hydrogen atoms and 1 oxygen atom are taken to form a water molecule.
This leaves a single oxygen atom forming a bond between the 2 glucose molecules which is called a glycosidic bond.

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13
Q
  • Explain the alterations made to the reducing sugar test to account for non-reducing sugars.
  • What molecules are non-reducing sugars?
A

An acid must be used to break down non-reducing sugars into reducing monosaccharides.
It must then be neutralised as the Benedict’s test cannot function in acidic conditions.

Polysaccharides and some disaccharides are non-reducing sugars, meaning they do not produce a colour change when mixed with Benedict’s solution.

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14
Q

Why do polysaccharides make good storage molecules?

A

They are long polymers of monosaccharide units. Due to their size, they are insoluble which means they do not affect the water potential of a cell. They are therefore valuable for storage.

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15
Q

Where is starch stored?
Where is glycogen stored?

A

Starch is stored as intracellular grains in plastids.
Glycogen is mainly stored as small granules in the muscles and liver.

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16
Q

Compare the structure of amylose to amylopectin.

A

Amylose is helically coiled with only alpha 1-4 glycosidic bonds.
Amylopectin is less coiled due to the presence of 1-6 bonds and is also more soluble than amylose.

17
Q

Describe 4 features of Starch that make it suitable for its function (storage).

A

• Coiled so compact.
• Insoluble so does not affect the water potential of a cell
• Branched so glucose can easily be released for respiration
• Large molecule so cannot travel across membranes / leave the cell

18
Q

Explain how glycogen differs from starch.

A

• It is found in animals & bacteria, unlike starch which is found in plants.
• It is more highly branched to allow for more glucose to be released faster.
• This is necessary as animals have higher metabolic rates.

19
Q

Describe 4 features of cellulose that make it suitable for its function.

A

• It is a long, linear chain of beta glucose molecules (joined by C1-4 glycosidic bonds after a condensation reaction).
• Layers are stacked in parallel, held together by bridging hydrogen bonds.
• Molecules form microfibrils & macrofibrils (which form cell walls when embedded in pectins).
• Strength is provided due to the abundance of bonds.

20
Q

How do the hydroxyl groups line up for a condensation reaction between 2 beta glucose monomers?

A

Like with alpha glucose molecules, the bonds are C1-4. Every 2nd beta glucose molecule is flipped upside down in order to align the hydroxyl groups to form a glycosidic bond.