Biology 1 Chapter 4 (Lecture) Flashcards

1
Q

Organisms are made up of chemicals that are based mostly on the element ___

A

Carbon

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2
Q

Organic Compounds

A

Compounds that contain carbon.

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3
Q

Organic Chemistry

A

The branch of chemistry that specializes in the study of carbon compounds.

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4
Q

The key to Carbon’s versatility

A

Is due to its electron configuration. It has 4 valence electrons that make it tend to form COVALENT bonds with or atoms by sharing its 4 electrons with other atoms. This may include SINGLE or DOUBLE bonds.

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5
Q

Carbon’s most frequent partners

A

Oxygen, Hydrogen, & Nitrogen

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6
Q

Carbon skeletons may vary in

A

1) Length
2) Branching
3) Double Bonds
4) Rings

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7
Q

CO2

A

O=C=O

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8
Q

Hydrocarbons

A

Organic molecules that consist of only C and H atoms. They are a major component of petroluem and fats (have long hydrocarbon tails). Neither hydrocarbons nor fats are soluble in water. They are hydrophobic; bonds are nonpolar. They can undergo reactions that release large amounts of energy.

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9
Q

Isomers

A

Compounds that have the same number of atoms of the same elements but different structures and hence different properties.

1) Structural Isomers
2) Geometric Isomers
3) Enantiomers

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10
Q

Structural Isomers

A

Differ in the covalent arrangements of their atoms.

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11
Q

Geometric Isomers

A

Have the same covalent partnerships, but differ in spatial arrangement due to inflexibility of the double bond.

1) Cis
2) Trans

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12
Q

Encantiomers

A

Mirror images; usually one biologically active; one inactive

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13
Q

Asymmetrical

A

The carbon attached to 4 different atoms or groups of atoms.

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14
Q

Functional Groups

A

Chemical groups that participate in chemical reactions in a characteristic way, from one organic molecule to another.

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15
Q

7 Chemical Groups that are important in biological processes

A

1) Methyl
2) Phosphate
3) Sulfhydryl
4) Amino
5) Carboxyl
6) Carbonyl
7) Hydroxyl

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16
Q

All 7 groups are…

A

Polar thus increasing the solubility of organic compounds in water.

17
Q

ATP

A

The organic phosphate has three phosphates present. When it reacts with water in the cell, a Phosphate is “split off” and energy is released. This energy is used in many cellular reactions.

18
Q

Phosphates Group

A
O
                    ||
Structure: -O-P-O-
                    ||
                    O-

Name: Organic Phosphate

Ex: Glyceral Phosphate

Functional Properties: Contributes regular charge to molecules it is a part of. Has potential to react with water to release energy.

19
Q

Amino Group

A
H
                   /
Structure: -N        
                   \
                     H
(-NH2)

Name: Amines

Ex: Glycine (Both amino & carboxylic acids)

Functional Properties: Acts as a base, Can pick up H+ from solution.

20
Q

Carboxyl Group

A
O
                   //
Structure: -C
                   \
                     OH
(-COOH)

Name: Carboxylic Acid

Ex: Acetic Acid (Vinegar)

Functional Properties: Acidic properties. This H can split off. H+ would increase [H+] in solution.

21
Q

Sulfhydryl Group

A

Structure: -SH

Name: Thiois

Ex: Cysteine

Functional Properties: 2 Sulfhydryl groups can react forming covalent bond, helps to stabilize proteins. (Perms in hair)

22
Q

Hydroxyl Group

A

Structure: R-C-OH

Name: Alcohols

Ex: Ethanol

Function Properties: Polar. Can form H bonds with water molecules helping them dissolve.

23
Q

Carbonyl Group

A

Structures: C=O and R-C=O

Names : C=O is Ketones (If C=O with C skeleton) and Aldehydes (If C=O is at the end)

Ex: Acetone (Ketones) and Propanol (Aldehydes)

Function Properties: Found in sugars.

24
Q

Flow of information in eukaryotic cells (Chapter 5)

A

DNA→RNA→Proteins

25
Q

Glycerol phosphate (Functional Group Example)

A

Phosphate

26
Q

Glycine (Functional Group Example)

A

Amino (Both carboxylic and amino)

27
Q

Acetic Acid (Functional Group Example)

A

Carboxyl

28
Q

Cysteine (Functional Group Example)

A

Sulhydral

29
Q

Alcohols (Functional Group Example)

A

Hydroxyl

30
Q

Acetone (Functional Group Example)

A

Carbonyl (Ketones)

31
Q

Propanol (Functional Group Example)

A

Carbonyl (Aldehydes)