Unit 1 (Chapter 3 Part 1) Flashcards

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1
Q

What is a carbon-containing molecule, so named because such molecules were first discovered in living organisms?

A

Organic molecule (contains carbon)

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2
Q

What are other organic molecules instead of carbohydrate, proteins, and nucleic acids?

A

Lipids

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3
Q

What was Vitalism?

A

Organic molecules could not be created and were a vital life force within living things.

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4
Q

How was Vitalism disproved?

A

Wohler accidentally created urea crystals which he studied extensively. This began the field of organic chemistry.

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5
Q

What is so special about the carbon atom?

A

It can form four covalent bonds.

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6
Q

What types of atoms does carbon bond to?

A

Bonds with other carbon, hydrogen, oxygen, nitrogen, and sulfur atoms.

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7
Q

What types of bonds is carbon capable of?

A

Single or double bonds.

Or, in the case of Carbon and Nitrogen, can be triple bonds.

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8
Q

What bonds with carbon are nonpolar?

A

Carbon and hydrogen (similar electronegativities) bonding and obviously with Carbon and Carbon bonding.

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9
Q

What do you call molecules with predominantly hydrogen–carbon bonds?

A

Hydrocarbons

Remember: They are poorly soluble in water and have extremely similar electronegativities.

Otherwise, formations with molecules such as oxygen or nitrogen, they are much more soluble in water.

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10
Q

What is another important feature of carbon?

A

Carbon bonds are stable within large temperature ranges.

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11
Q

Why are carbon bonds more stable in a large range of temperatures (frigid poles and superheated deep-sea vents)?

A

Since Carbon atoms are relatively small, their bonds are incredibly short which makes them much stronger. Longer bonds tend to form between larger atoms.

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12
Q

What is a group of atoms with a characteristic chemical structure that exhibits particular properties?

A

Functional Groups

Each functional group exhibits the same properties in all molecules in which it occurs.

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13
Q

Bonus: What does the R mean in chemical formulas?

A

A radical.

It is an abbreviation for any group in which a carbon or hydrogen atom is attached.

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14
Q

What are some functional groups, where they might be found, and their properties?

A

Amino - Amino acids (proteins) // Weakly basic (can accept H+); polar; forms part of peptide bonds

Carbonyl - Steroids, waxes, and proteins // Polar; highly chemically reactive; forms hydrogen bonds

Aldehyde - Linear forms of sugars and some odor molecules // Polar; highly chemically reactive; forms hydrogen bonds

Carboxyl - Amino acids, fatty acids // Acidic (gives up H+ in water); forms part of peptide bonds

Hydroxyl -
Steroids, alcohol, carbohydrates, some amino acids // Polar; forms hydrogen bonds with water

Methyl - May be attached to DNA, proteins, and carbohydrates // Nonpolar

Phosphate - Nucleic acids, ATP, phospholipids // Polar; weakly acidic and negatively charged at typical pH of living organisms

Sulfate - May be attached to carbohydrates, proteins, and lipids // Polar; negatively charged at typical pH of living organisms

Sulfhydryl - Proteins that contain the amino acid cysteine // Polar; forms disulfide bridges in many proteins

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15
Q

What is an isomer?

A

Two or more molecules with the same chemical formula but different structures and characteristics.

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16
Q

What are isomers that contain the same atoms but in different bonding relationships?

A

Structural isomers.

Much like urea and ammonium cyanate. Or like isopropyl alcohol and propyl alcohol.

17
Q

What are isomers with identical bonding relationships, but different spatial positioning of their atoms?

A

Stereoisomers

18
Q

What are the two types of stereoisomers?

A

Cis-trans isomers and enantiomers.

19
Q

What are organic molecules with the same chemical composition but existing in two different configurations determined by the positions of hydrogen atoms on the two carbons of a C═C double bond?

A

Cis/trans isomers.

When the hydrogen atoms are on the same side of the double bond, it is called a cis isomer; when on the opposite sides of the double bond, it is a trans isomer.

20
Q

What is the most notable property of a cis/trans isomer?

A

Their stability and sensitivity to heat and light.

For example, the light sensitive region of your eye contains a molecule called retinal, which exists in either a cis or trans form. In darkness, the cis-retinal form predominates. The energy of sunlight, however, causes retinal to isomerize to the trans form. The trans-retinal activates the light-capturing cells in the eye.

21
Q

What isomer is one of a pair of stereoisomers that exist as mirror images?

A

Enantiomer.

You can think of these as a pair of gloves. No way you hold the left-handed glove, it will never fit the right hand.

Another example… An enzyme that recognizes one enantiomer usually does not recognize the other.

22
Q

Some organic molecules are extremely large. How do these molecules link together?

A

They use organic molecules called a Monomer (meaning one part).

This is used to form a larger molecule called a polymer which consists of many repeating units of the monomer.

23
Q

What is a large molecule formed by linking many smaller molecules called monomers?

A

A polymer (meaning many parts).

24
Q

What is a chemical reaction in which two or more molecules are combined into one larger molecule by covalent boning, with the loss of a small molecule?

A

Condensation reaction.

This produces a larger organic molecule plus a water molecule.

25
Q

What is another name for condensation reaction and why?

A

Dehydration reaction because a molecule of water is lost.

26
Q

T/F Polymers can reach great lengths, much like DNA, by the process of dehydration reactions up to millions of monomers called nucleotides.

A

True

27
Q

What is an example of an unstable polymer unlike the stable polymer of DNA?

A

Carbohydrates

28
Q

What is the process by which a polymer is broken down into monomers?

A

A hydrolysis reaction.

This is a chemical reaction that utilizes water to break apart other molecules.

In the example of a carbohydrate, plants store them as starches, which use hydrolysis reactions to break them down into their constituent monomers for energy.

29
Q

What are the four broad categories of organic molecules and macromolecules in all forms of life based on their chemical and biological properties?

A

Carbohydrates, Lipids, Proteins, and Nucleic acids.