Ch 15 organic compounds Flashcards

1
Q

what type of bonds do carbons create?

A

max of 4 covalent bonds that are short and strong

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2
Q

define catenation

A

ability of a C to bond to C

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3
Q

heteroatoms

A

atoms other than C and H, usually N and O but also P and S

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4
Q

reactivity of C-C

A

EN valences equal, nonploar, unreactive

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5
Q

reactivity of C-H

A

short bond, nearly non polar, largely unreactive

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6
Q

reactivity of C-O

A

highly polar change in EN=1 with O e- rich and C e- poor

Reactive and easy to break

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7
Q

reactivity of C-heteroatoms

A

heteroatoms are generally large so regardless of EN, chains are long and easy to break

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8
Q

define functional group

A

specific combo that reacts in a characteristic manner

- this is where reactions of organic compounds occur

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9
Q

Types of hydrocarbons

A

alaphatic and aromatic

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10
Q

types of alaphatic hydrocarbons

A

alkanes, cycloalkanes, alkenes, alkynes

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11
Q

What are alkanes

A

hyrdocarbons with ONLY single bonds

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12
Q

alkane formula

A

Cn+H(2n+2)

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13
Q

in alkanes, how are carbons hybridized?

A

sp3

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14
Q

define saturated hydrocarbons

A

When Carbon is bonded to the max

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15
Q

When naming, what does the root identify?

A

of Cs in longest continuous chain

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16
Q

When naming, ,what does the suffix identify?

A

type of hydrocarbon or key functional group

17
Q

When naming, what does the prefix identify? what do you add?

A

branches on the main chain and the # of carbons that branch has
add -yl to root name

18
Q

meth-

A

1

19
Q

eth-

A

2

20
Q

prop-

A

3

21
Q

but-

A

4

22
Q

pent-

A

5

23
Q

hex-

A

6

24
Q

hept-

A

7

25
Q

oct-

A

8

26
Q

non-

A

9

27
Q

dec-

A

10

28
Q

can sigma bonds rotate?

A

yes

29
Q

can pi bonds rotate?

A

no