Concept 4.2: Carbon atoms can form diverse molecules by bonding to four other atoms

0.0(0)
Studied by 0 people
call kaiCall Kai
Locked
learnLearn
examPractice Test
spaced repetitionSpaced Repetition
heart puzzleMatch
flashcardsFlashcards
GameKnowt Play
Card Sorting

1/10

flashcard set

Earn XP

Description and Tags

Flashcards from Concept 4.2 of Pearson's Campbell Biology, Twelfth Edition.

Last updated 4:03 AM on 7/16/26
Name
Mastery
Learn
Test
Matching
Spaced
Call with Kai
Chat

No analytics yet

Send a link to your students to track their progress

11 Terms

1
New cards

Electron configuration

How an atom’s electrons are arranged; the key to atomic bond types and numbers as part of their characteristics

2
New cards
<p>Carbon</p>

Carbon

An atom with four valence electrons that can form four covalent bonds

  • Molecules with multiple of these have a tetrahedral shape when joined to four other atoms

  • Two of these together in a double bond allow other atoms to stay in the same plane

3
New cards
<p>Valence</p>

Valence

The number of unpaired electrons in the valence shell of an atom, determining the number of covalent bonds it can form

4
New cards

Carbon bonding partners

Most frequent are:

  • Hydrogen

  • Oxygen

  • Nitrogen

5
New cards

Carbon molecule examples

  • Carbon dioxide: CO2

  • Urea: CO(NH2)2

  • Estradiol and Testosterone

6
New cards
<p>Carbon chains</p>

Carbon chains

The skeletons of most organic molecules that vary in length, shape, double bond position, branches, and ring presence

7
New cards
<p>Hydrocarbons</p>

Hydrocarbons

Organic molecules consisting of only carbon and hydrogen

  • Many organic molecules, such as fats, have these as they can release a large amount of energy in some reactions

8
New cards
<p>Isomers</p>

Isomers

Compounds with the same molecular formula (ratio) but different structures (arrangements) and properties, includes:

  • Structural: Different covalent bonds and arrangements

  • Cis-trans: Differing spatial arrangements, same covalent bonds

  • Enantiomers: Mirror images

9
New cards
<p>Structural isomers</p>

Structural isomers

Isomers with different covalent bonds and arrangements

10
New cards
<p>Cis-trans isomers</p>

Cis-trans isomers

Isomers with the same covalent bonds but differing spatial arragnements

11
New cards
<p>Enantiomers</p>

Enantiomers

Isomers that are mirror images of each other

  • Important in the pharmaceutical industry, as each pair may have different effects or not be effective at all, demonstrating molecular sensitivity

  • Ibuprofen’s and albuterol’s versions are ineffective