Chapter Two Flashcards

1
Q

Hydrocarbon :

A

molecules with only carbons and hydrogens

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2
Q

Alkanes:

A
  1. type of hydrocarbon
  2. does not have any functional group
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3
Q

Functional group

A

Part of the molecule where
a chemical reaction occurs

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4
Q

General formula for alkanes

A

CnH2n+2

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5
Q

Methane

A

CH4

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6
Q

Ethane

A

Ch3-Ch3

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7
Q

Propane

A

Ch3-Ch2-ch3

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8
Q

Butane

A

Ch3-Ch2-ch2-ch3

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9
Q

what are some features of Alkane:

A
  1. insoluble in water
  2. good lubricants and protecting metals surface from corrosion
  3. non polar
  4. soluble in nonpolar or organic solvent
  5. have densities lower than
    water = 0.6-0.8 g/mL
  6. Boiling points of continuous Alkanes
    increase with an increase in carbon
    chain length
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10
Q

what are the steps to name an organic compound:

A

Rule 1: Find the longest continuous chain of carbon atoms and use the name of this chain
as the base name of the compound
2. Rule 2: Number the longest chain, beginning with the end of the chain nearest a
substituent
3. Rule 3: Name the groups attached to the longest chain as alkyl groups. Give the location of
each alkyl group by the number of the main-chain carbon atom to which it is attached

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11
Q

Constitutional isomers

A

Structural isomers
= compounds with the same molecular formula
but the carbons are connected differently

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12
Q

Conformation

A

different arrangements of atoms caused by rotation of a single bond

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13
Q

what are forms are conformation?

A

Staggered & Eclipsed

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14
Q

T/F: Pure conformers cannot be isolated in most cases, because the molecules
are constantly rotating through all the possible conformations

A

True

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15
Q

Which conformer is more stable?

A

Most stable
conformer
is staggered

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16
Q

Newman projection

A

The Newman projection is the best way to judge the stability of the
different conformations of a molecule

17
Q

Butane has two different staggered conformations, explain

A

gauche (60° between the methyl
groups) and anti (180° between the methyl groups)

18
Q

T/F:The eclipsed conformation where the dihedral angle between the methyl groups is 0° is
referred to as totally eclipsed

A

True

19
Q

Newman Projection: steps

A

1) Determine which bond is being considered
2) Determine which atom is front atom of bond being considered
3) The substituents attached to the front atom are drawn to a point,
the substituents attached to the back atom are drawn to a circle
4) The relative angles and orientation of the substituents are
maintained

20
Q

Cycloalkane

A

Cyclic Hydrocarbon without functional group, general formula: CnH2n

21
Q

what are the factors that affect stability in cycloalkanes?

A

Angle strain, & Torsional strain

21
Q

what are the features of cycloalkanes:

A

Nonpolar
-Not soluble in water
-Density similar to alkanes
-Boiling point depends in
ring size

21
Q

Angel Strain

A

from the compressing of the bond angles

21
Q

Torsional strain

A

from eclipsing of the bonds

22
Q

The most stable conformation of cyclohexane is
the chair form shown to the right. The C-C-C bonds are
very close to 109.5o, so it is almost free of angle strain.
It is also a fully staggered conformation and so is free of
torsional strain

A

True

23
Q

Stereoisomers

A

Same connectivity (not constitutional isomers),
but differing arrangement in space

24
Q

stereoisomers are :

A
  1. Cis: same side
  2. Trans: Opposite side