Chapter 4: Carbon and the Molecular Diversity of Life

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Last updated 10:14 PM on 1/28/26
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30 Terms

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carbon electron configuration

  • 2 elects in the first shell and 4 in the second

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carbon’s chemical reactivity

  • never really loses or gains 4 electrons → completes its valence shell by sharing electrons → 4 covalent bonds

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carbon forms what kind of bonds?

single and double covalent

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what shape does a molecule with multiple carbon atoms create?

tetrahedral

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what shape does a two carbon atom joined by a double bond create?

bonds lie in the same plane

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the number of unpaired electrons in the valence shell of an atom is equal to…

the valence and number of covalent bonds

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what are the most frequent bonding partners of carbon…

hydrogen, oxygen, and nitrogen

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hydrocarbons

organic molecules made up of only carbon and hydrogen

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hydrocarbons are a major component of

petroleum

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fats

contain long hydrocarbon tails and the tails are attached to a non-hydrocarbon component

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petroleum and fats are

hydrophobic (bc their many non polar carbon-hydrogen bonds)

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hydrocarbons can undergo reactions and release

a large amount of energy

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isomers definition

compounds with the same molecular formula BUT different structures → which leads to different chemical properties

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cis-trans isomers (geometric isomers)

same covalent partnerships

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cis-trans isomers (geometric isomers)

differ in spatial arrangement and their double bond restricts rotation(lock atoms in specific positions)

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Enantiomer definition

isomers that are mirror images of each other

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Enantiomers conditions formation

occurs when an asymmetric carbon is present and bonded to 4 diff atoms or groups (four groups can be arranged in two distinct spatial configurations that are non-superimposable mirror images)

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bio activity of enantiomer

only 1 enantiomer is active at a time and the other enantiomer is inactive or functionally different

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functional significance of enantiomer

small differences between enantiomers can lead to major functional changes → due to emergent properties that arise from the specific 3D arrangement

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the unique properties of an organic molecule depend on

arrangement of its carbon skeleton and the chemical groups attached to that skeleton

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the chemical groups

contribute to each molecule’s distinct characteristics and can replace hydrogen atoms in hydrocarbons

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chemical groups can

  • be involved in chemical reactions

  • affect the shape and function of the molecule

  • give the molecule its unique properties

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ex (of chemical groups) : steroid hormones

testosterone and estradiol → same basic carbon skeleton, BUT differ in chemical groups attached, shape, and biological effects

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functional groups

  • Hydroxyl group

  • Carbonyl group

  • Carboxyl group

  • Amino group

  • Sulfhydryl group (HYDROPHOBIC)

  • Phosphate group

  • Methyl group (NON-REACTIVE)

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ATP

important to organic phosphate and is the primary energy transfer molecule in living cells

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ATP is made of

organic molecule called adenosine

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when ATP reacts with water

One phosphate group is removed → molecule becomes ADP

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ATP (storage)

“store“ energy→holds the potential to release energy when reacting with water

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ATP (release)

released energy is used to power various cellular processes