Chapter 4 - Carbon and Molecular Diversity Flashcards

1
Q

Formation of Bonds with Carbon

A
  • Carbon has 6 electrons; 2 in the first shell and 4 in the valence shell
    - Usually completes its valence by sharing 4 covalent bonds
    • When carbon atoms form 4 single covalent bonds, the arrangement of the 4 orbitals(space for electrons to float within) angle to form an imaginary tetrahedron
    • But when two carbon atoms are joined by a double bond, the bonds are in the same plane, so the atoms which joined to the carbons fall into the same plane
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2
Q

Rules for Bonding for CO2

A
  • In Co2, two oxygens are double bonded to carbon
    • The two double lines have the same number of shared electrons as 4 single bonds, completing the valence shell of the carbon
  • Co2 is often called inorganic because it is simple and lacks hydrogen
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3
Q

Rules of Bonding for Urea CO(NH2)2

A
  • It is an organic compound found in urine
    • Carbon is participating in both single and double bonds to fill its valence shell
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4
Q

Carbon Skeleton

A

the backbone of molecules and are the chains which form the basis of most organic molecules

- Can vary in length and can be straight, branched, or closed rings and can have single or double bonds
- The variation in carbon chains is important for molecular diversity and complexity
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5
Q

Hydrocarbons

A

an organic molecule consisting of only hydrogen and carbon atoms
- The major components of petroleum and fats
- Not prevalent in most livign organisms
- Can undergo reactions which release a relatively large amount of energy

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6
Q

Isomers

A

one of two or more compounds which have the same number of atoms of the same elements but different structures and therefore different properties

  • structural, geometric or Enantiomers
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7
Q

Types of Isomers: Structural

A

a compound which has the same molecular formula but differs due to the covalent arrangement of their atoms
- The bigger the carbon skeleton, the more the possible isomers
- Can also differ in the location of double bonds

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8
Q

Types of Isomers: Geometric

A

have the same molecular formular and covalent bonds between atoms but differ in the spatial arrangement of the atoms due to the inflexibility of double bonds
- Occurs when a carbon is double bonded to a carbon each with their own two atoms, then distinct cis-trans isomers are possible

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9
Q

Types of Geometric Isomers

A

Cis Isomers: the two R groups are on the same side of the carbon-to-carbon double bond

Trans Isomers: the two R groups are on opposite sides of the carbon-to-carbon double bond

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10
Q

Types of Isomers: Enantiomers

A

isomers which are mirror images of each other but differ in shape due to the presence of an asymmetric carbon
- Similar to hands and gloves, the ‘left handed’ molecule cant do the job of the ‘right handed’ molecule

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11
Q

Functional Groups

A

chemical groups(a specific configuration of atoms) which are directly involved in Chemical Reactions

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12
Q

Hydroxyl Group

A

-OH

  • polar(electronegative O) and forms hydrogen bonds with water and helps dissolve compounds
    • Types of alcohol molecules(ending in -ol)
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13
Q

Carbonyl Group

A

C=O

  • fall either within Carbon Skeletons (ketones)
    • Fall at the end of Carbon Skeletons (aldehydes)
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14
Q

Carboxyl Group

A

OH- C=O

  • acts as an acid(can donate H+) because of polar bond between O and H creating -1 charge
    • Found in Any type of acid
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15
Q

Amino Group

A

NH2

  • acts as a base and can pick up H+ from surrounding solutions creating a +1 charge
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16
Q

Sulfhydryl Group

A

-SH

  • two can form crosslinks which stabilize protein structures(E.g. help DNA keep its helix shape by forming bonds)
    • Named Thiols
17
Q

Phosphate Group

A

O-P=O - O2-

  • confers on to molecules the ability to react with water(gives energy)
    • adds negative charges when inside a chain
    • adds 2 negative charges when at the end of a chain
18
Q

Methyl Group

A

C - H3

  • Doesn’t provide properties but serves as recognizable tags on biological molecules to signal ‘self DNA’