Org Chem Flashcards

1
Q

Alkanes can react with halogens in the presence of UV light to form an acid and a substituted alkane (a haloalkane).

A

Free radical substitution

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2
Q

is called a concerted reaction. No matter how many bonds are broken or formed, a starting material is converted directly to a product.

A

one-step reaction

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3
Q

a carbon atom surrounded by only six electrons; is an electrophile

A

Carbocation

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4
Q

is the minimum amount of energy needed to break bonds in the reactants. It represents an energy barrier that must be overcome for a reaction to occur.

A

Energy of activation

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5
Q

The angle that separates a bond on one atom from a bond on an adjacent atom is called a

A

dihedral angle

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6
Q

a negatively charged carbon atom; is a nucleophile

A

Carbanion

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7
Q

The C-H bonds on one carbon bisect the H-C-H bond angle on the adjacent carbon.

A

Staggered conformation

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8
Q

The C-H bonds on one carbon are directly aligned with the C-H bonds on the adjacent carbon.

A

Eclipsed conformation

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9
Q

breaking a bond by unequal division of electrons between the two atoms in the bond. Electrons normally end up on the more electronegative atom.

A

Heterolysis or heterolytic cleavage

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10
Q

X atom is bonded to the carbon atom adjacent to a carbon-carbon double bond.

A

Allylic halides

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11
Q

are nucleophiles because they contain a carbon with a lone pair.

A

Carbanions

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12
Q

is a reaction in which elements of the starting material are “lost” and a pi bond is formed. These reactions are the complete opposite of addition reactions.

A

Elimination

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13
Q

Physical properties of alkyl halides

A
  1. Weakly polar molecules
    2.Dipole-dipole interactions because of their polar cx bond
  2. Incapable of intermolecular hydrogen bonding because the rest of the molecule contains only CC & CH bonds
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14
Q

A staggered conformation with two larger groups of 180° from each other is called

A

anti

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15
Q

Shows movement of an electron pair

A

Full-headed curved arrow

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16
Q

is an increase in energy resulting when atoms are forced too close to one another.

A

Steric strain

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17
Q

Is produced by a giant kelp and algae and also found in emissions from volcanoes such as Hawaii’s Kilauea

A

Chloromethane

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18
Q

X atom is bonded to the carbon atom adjacent to a benzene ring.

A

Benzylic halides

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19
Q

is a substance that speeds up the rate of a reaction.
is recovered unchanged in a reaction, and it does not appear in the product.

A

catalyst

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20
Q

X atom is bonded to a carbon-carbon double bond.

A

Vinyl halides

21
Q

Drawn between the starting materials and products in an equation

A

Reaction arrow

22
Q

breaking a bond by equal division of electrons between the two atoms in the bond.

A

Homolysis or homolytic cleavage

23
Q

Is an important solvent, once used to decaffeinate coffee.

A

Dichloromethane

24
Q

Shows movement of a single electron

A

Half-headed curved arrow

25
The energy difference between the transition state and the starting material is called
the energy of activation, symbolized by Ea
26
involves more than one step. A starting material is first converted to an unstable intermediate, called a reactive intermediate, which then goes on to form the product.
stepwise reaction
27
are highly unstable because they contain an atom that does not have an octet of electrons.
Radicals
28
- are aliphatic hydrocarbons having only C-C and C-H sigma bonds - can be categorized as cyclic or acyclic
Alkanes
29
are organic molecules containing a halogen atom X bonded to an sp3 hybridized carbon atom.
Alkyl Halides
30
is the energy needed to homolytically cleave a covalent bond to form two radicals.
Bond Dissociation Energy
31
contain carbons joined together in one or more rings. Their general formula is CnH2n.
Cycloalkanes
32
Drawn between resonance structures
Double-headed arrow
33
is a compound secreted by cockroaches. It is a pheromone, a chemical substance used for communication in an animal species, commonly among insects.
Undecane
34
are electrophiles because they contain an electron-deficient carbon.
Radicals and carbocations
35
is the slowest step of a chemical reaction that determines the speed at which the overall reaction proceeds.
rate determining step
36
generates charged intermediates called ions.
Heterolysis
37
Is a safe general anesthetic that has now replaced other organic anesthetics such as CHCL3 which causes liver and kidney damage
Halothane
38
generates uncharged reactive intermediates with unpaired electron called radicals.
Homolysis
39
The energy absorbed or released in any reaction is called
the enthalpy change or heat of reaction.
40
are organic molecules containing a halogen atom X bonded to an sp3 hybridized carbon atom. can be classified as primary, secondary or tertiary.
Alkyl Halides (R-X)
41
A staggered conformation with two larger groups of 60° from each other is called
gauche
42
is a reaction in which an atom or a group of atoms is replaced by another atom or group of atoms.
Substitution
43
have the molecular formula CnH2n+2. Also called saturated hydrocarbons because they have the maximum number of hydrogen atoms per carbon.
Acyclic alkanes
44
Drawn between the starting materials and products in an equilibrium equation
Double reaction arrows
45
are different arrangements of atoms that are interconverted by rotation about single bonds.
Conformations
46
is a reaction in which elements are added to a starting material. These reactions occur when two reactants add together to form a single product with no atoms “left over”.
Addition
47
X atom is bonded to a benzene ring.
Aryl halides
48
is one of the components in mangoes.
cyclohexane