Chemistry: Carbon and Organic Molecules

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Questions and Answers

Which of the following best describes the effect of a double bond on the rotation of a carbon molecule?

  • Has no impact on the molecule's rotation.
  • Allows for free rotation, similar to a single bond.
  • Increases the speed of rotation compared to a single bond.
  • Significantly restricts rotation, creating a planar structure. (correct)

How does the presence of an amino group impact the pH of a solution?

  • It decreases the concentration of hydrogen ions, thus increasing the pH. (correct)
  • It neutralizes the pH, bringing it to 7.
  • It has no effect on the pH of the solution.
  • It increases the concentration of hydrogen ions, thus lowering the pH.

If a carbon molecule has the structure $CH_3-C-CH_3$, while comparing it to the structure $C_2H_5-C-C_2H_5$, which difference is most likely to occur

  • The structures are isomers of each other, but have no other structural differences.
  • The first would be a stereoisomer while the second structure would be an enantiomer
  • The structures are structural isomer of each other. (correct)
  • The first structure is an enantiomer, and the second is a structural isomer.

Which functional group is likely to create a disulfide bridge when forming proteins?

<p>Sulfhydryl group (-SH). (A)</p> Signup and view all the answers

What characteristic is most likely to make a molecule a hydrocarbon?

<p>The presence of non-polar covalent bonds between carbon and hydrogen. (A)</p> Signup and view all the answers

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Flashcards

Covalent bond

A chemical bond formed by the sharing of electron pairs between atoms.

Isomers

Molecules with the same chemical formula but different structural arrangements.

Carbonyl group

A functional group consisting of a carbon atom double-bonded to an oxygen atom.

Amino group

A functional group consisting of a nitrogen atom bonded to two hydrogen atoms.

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Sulfhydryl group

A functional group consisting of a sulfur atom bonded to a hydrogen atom.

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Study Notes

Carbon

  • Carbon has 4 valence electrons
  • Carbon forms the backbone of many organic molecules
  • Carbon-containing molecules are organic molecules
  • Carbon forms covalent bonds
  • Carbon bonding involves hybridization of orbitals
  • Carbon forms different shapes depending on bonding (tetrahedral, trigonal planar, etc.)

Organic Molecules

  • Organic molecules contain carbon
  • Organic molecules show diverse structures and properties
  • Different structures impact properties (e.g., isomers)

Bond Types

  • Covalent bonds (sharing electrons)
  • Single bonds allow for rotation
  • Double bonds do not allow for rotation
  • Triple bonds are linear

Isomers

  • Isomers have the same chemical formula but different structures
  • Structural isomers have different bonding arrangements
  • Stereoisomers have different spatial arrangements around a central bond (geometric/cis-trans, enantiomers)
  • Geometric isomers differ in the arrangement around a double bond (cis-trans)
  • Enantiomers are mirror images of each other

Functional Groups

  • Hydroxyl (-OH): polar covalent bond, hydrophilic, alcohols
  • Carbonyl (C=O): aldehydes, ketones
  • Carboxyl (-COOH): acids, increase acidity
  • Amino (-NH2): bases, increase pH
  • Sulfhydryl (-SH): cysteine, disulfides
  • Methyl (—CH3): nonpolar, hydrophobic
  • Phosphate (-PO4): reacts with water, energy transfer

Other Notes

  • Silicon is in the same family as carbon but has different reactivity with oxygen
  • Hydrocarbons are nonpolar molecules

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