Carbohydrates Flashcards

memo (48 cards)

1
Q

What are the 2 types of Biochemical substances?

A

Bioinorganic Substances and Bioorganic Substances

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2
Q

Biochemical substances that DO NOT contain Carbon

A

Bioinorganic Substances

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3
Q

Biochemical Substances that contains Carbon

A

Bioorganic Substances

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3
Q

What are the 2 Bioinorganic Substances?

A

water and inorganic salts

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3
Q

-The most abundant class of bioorganic molecules on planet Earth.
-It constitute about 75% by mass of dry plant materials.

A

Carbohydrates

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3
Q

What are the 4 Bioorganic substances?

A

Proteins, Lipids, Carbohydrates, Nucleic Acids

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3
Q

the provides energy reserves for the plants in plants?

A

starch

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3
Q

it serves as the structural elements in plants?

A

cellulose

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4
Q

Plants have two main uses for the carbohydrates they produce. What are they?

A

Starch and Cellulose

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4
Q

What are the 4 classification of carbohydrates?

A

Monosaccharides, Disaccharides, Oligosaccharides, Polysaccharides

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4
Q

Enumerate 3 MONOSACCHARIDES

A

Glucose, Fructose, Galactose

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4
Q

Enumerate 3 DISACCHARIDES

A

Sucrose, Lactose, Maltose

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5
Q

Enumerate 2 OLIGOSACCHARIDES

A

Trisaccharides, Tetrasaccharides

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6
Q

Enumerate 3 POLYSACCHARIDES

A

Cellulose, Starch, Glycogen

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7
Q

What are the composition of Sucrose

A

1 Glucose and 1 Fructose

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8
Q

What are the composition of Lactose

A

1 Glucose and 1 Galactose

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9
Q

What are the composition of Maltose

A

2 Glucose

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10
Q

Examples of Trioses

A

Glyceraldehyde [aldotriose] and Dihydroxyacetone [ketotriose]

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11
Q

Examples of Tetroses

A

Erythrose [aldotetrose] and Erythulose [ketotetrose]

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12
Q

Examples of Pentoses

A

Ribose [aldopentose] and
Ribulose [ketopentose]

12
Q

Examples of Hexoses

A

Glucose, Galactose, Mannose [aldohexose] and Fructose [ketohexose]

12
Q

Examples of Heptoses

A

Sedoheptulose and Mannoheptulose

13
Q

-are images that coincide at all points when the images are laud upon each other.

A

Superimposable

13
Q

-are images where NOT all points coincide when the images are laid upon each

A

Nonsuperimposable

13
is an atom in a molecule that has four different groups bonded to it in a tetrahedral orientation.
Chiral Center
14
the handedness-generating carbon atom.
Chiral Center
15
is a molecule whose mirror image are superimposable.
Acharial Center
16
is a molecule whose mirror images are not superimposable.
Chiral Center
17
How can we identify a Chiral Centel
To have four groups present, all bonds about the chiral center must be single bond.
18
why is chirality important?
- response of body to the right-handed form of the hormone epinephrine is 20 times greater than its response to the left- handed form.
18
isomers with a different connectivity
Constitutional Isomers
18
different compounds with the same molecular formula
Isomers
19
isomers with the same connectivity but a different orientation of their atoms in space
Stereoisomers
20
Types of stereoisomers
Enantiomers and Diastereomers
21
what does "enantios" mean?
Opposite
22
whose molecules are nonsuperimposable mirror images of each other (L and R handed forms of a molecule with a single chiral center).
Enantiomers
23
molecules are not mirror images of each other ( contain more than one chiral center).
Diastereomers
23
German chemist and the developer of the two-dimensional system for specifying chirality
Hermann Emil Fischer
23
awarded the second Nobel prize in chemistry
Hermann Emil Fischer
24
British carbohydrate chemist. Determine the structures of the cyclic forms of glucose
Walter Norman Haworth
24
In what year was Hermann Emil Fischer awarded the second Nobel prize in chemistry?
1902
25
Co-recipient of the 1937 Nobel prize in Germany
Walter Norman Haworth
26
what formula did Walter Norman Haworth develop?
Haworth Projection Formula
27
MONOSACCHARIDE oxidation can yield/produces three different types of acidic sugars, what are the 3?
Gluconic acid Glucaric acid Glucuronic acid
28
oxidize the aldehyde end of an aldose to give an
ALDONIC ACID
29
it is a two dimensional structural notation that specifies the three dimensional structure of a cyclic form of a monosaccharide.
Haworth Projection Formula
30
Oxidize both ends of a monosaccharide at the same time (the carbonyl group and the terminal primary alcohol group)
ALDARIC ACID
31
oxidize the primary alcohol end of an aldose such as glucose, w/o oxidization of the aldehyde group, to produce an
ALDURONIC