Organic Chemistry Flashcards

1
Q

Molecular formula

A

The actual number of atoms of each element in a molecule

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2
Q

Structural formula

A

Shows the arrangements of atoms carbon by carbon with the attached hydrogens and functional groups

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3
Q

Skeletal

A

Shows the bonds of the carbon skeleton only with functional groups

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4
Q

Displayed formula

A

Shows how all the atoms are arranged and the bonds between them

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5
Q

Functional group

A

Group of atoms responsible for its characteristic reactions

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6
Q

Homologous series

A

Family of compounds that have the same functional group and general formula with each successive member differing by CH2

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7
Q

What is homolytic fission

A

Is the breaking of covalent bonds which forms 2 radicals with one electron from the bond going to each atom

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8
Q

Why are lots of products produced in radical substitution

A

As more than one substitution happens so more termination steps occur

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9
Q

Why is x and example of honolytic fission

A

As one electron from bond pair goes to each atom

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10
Q

What is an electrophile

A

Electron pair acceptors

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11
Q

WHat is a nucleophile

A

Electron pair donors

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12
Q

Alicyclic

A

An aliphatic compound arranged in non aromatic rings(ring like structure)

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13
Q

Aromatic

A

Contains benzene ring

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14
Q

Aliphatic

A

A compound containing carbon and hydrogen arranged in straight or branched chains

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15
Q

Alkyl

A

A hydrocarbon chain w general formula CnH2n+1

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16
Q

Heterolytic

A

The bond beaks unevenly with one of the bonded atoms receiving both electrons from the bonded pair

17
Q

Why is e/z isomerism shown

A

Due to carbon double bond which restricts rotation. Each carbon of the double bond is attached to two different groups

18
Q

Stereoisomerism

A

Same structural and molecule formula but different arrangement of atoms in space

19
Q

how are pi bonds formed

A

pi bonds are formed by the sideways overlap of 2 p orbitals in each carbon atom.Its formed above and below the atom

20
Q

j

A

j

21
Q

difference between pi and sigma bond

A

pi bond has a lower bond enthalpy .sigma bonds form between atoms and pi bonds form above and below atoms

22
Q

why does cracking form lots of products

A

as any cc bond in alkane can break

23
Q

why does this(a compound with 2 double bonds) not have cis/trans isomerism

A

as the c in the c=c bond are joined to two groups that are the same

24
Q

temp and conditions needed to make a polymer

A

ziegler catalyst with high temperature