1.5 Flashcards

1
Q

carbonyl group

A

carbon double bonded to an O, functional group responsible for properties in aldeydes and ketones

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2
Q

methanal

A

formaldehyde

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3
Q

aldehydes

A

terminal carbonyl group

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4
Q

ketones

A

non-terminal cabonyl group

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5
Q

properties of ketones and aldehydes

A

polar due to c-o bonds (D-D), stonger than alkanes but weaker than alchohols, lower boilng point and less soluble than alcohols, good solvents due to ability to dissolve polar and non-polar which depends on how big R group is, small aldehydes/ketones = completely soluble, size ++ = solubility down

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6
Q

reactions of carbonyl groups

A

controlled oxidation and hydrgoenation

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7
Q

controlled oxidation

A
primary alcohols = aldehyde + water
secondary = ketone + water
tertirary = no reaction
alcohol  =(O) aldehyde/ ketone + water
(o) = oxidzing agent = oxygen rich compounds = cr2o72- and KMnO4
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8
Q

hydrogenation

A

need high temp, preassure + catalyst

aldehyde/ ketone + h2 = alcohol

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9
Q

carboxylic acid

A

weak acid with a carbonyl and alcohol group attaches, sour/ tangy taste, polar, strong h-bonding and dipole-dipole, small Ca are soluble in water but solubility decreases as size does, higher melting, bigger np end = more ld, neutralizes

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10
Q

ester

A

organic compound cotnaining a carbonyl group bonded to a O bonded to a R group, responsible for odour and flavourings, no hydroxyl group = less polar than ca = no H-bonding, small ester are more soluble in water due to polarity of c-o bonds. less soluble than Ca + lower boiling, polarity = similar to aldehyde/ketones, organic salt

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11
Q

ester reactions

A

esterfication, hydrolysis and saponification

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12
Q

ca reactions

A

contorlled oxidization of a aldhyde

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13
Q

esterfication

A

ca + alcohol with h2so4 makes ester + water

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14
Q

hydrolysis

A

ester + strong base = alcohol + salt of acid

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15
Q

nh

A

amino functional group

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16
Q

adrenline

A

epinephrine

17
Q

amine

A

oraginc compound relates to ammonia which has an N boned to an alkyl group, polar, strong unpleasant odour as fishy, offensive decay and decomp odour, n-h bonds allow h-bonidng, higher boiling than similar sized hydrocarbons, smaller = more soluble, weak bases that neturalize, found in plants and have medicinal properties

18
Q

degree of amines

A

primary has the most h-bonding where as 3 has none

19
Q

amide

A

ca + amine, caontains a cabronyl group bonded to a N, weak base, insoluble in water, small = slightly soluble, acetaminophen, urea

20
Q

main component in pain killers

A

acetaminophen

21
Q

found in urine of mamals and used as a fertlizer

A

urea

22
Q

amine reaction

A

preperation - alkyl halide + ammonia/1 or 2 amine = amien + h___

23
Q

amide reactions

A

condensation reaction - ca + amine = amide + water

hydrolysis - amide + water = ca + amine

24
Q

3 types of linkages

A

c-c (playstic), c-o (ester) and c-n (Amine)

25
Q

polymer

A

large molecule made up of repeating monomer sequences

26
Q

types of polyemers

A

homopolymers (only one type of monomer, can only do add reactions) and copolymers (two types, add and condestaion reactions)

27
Q

addition polymer reactions

A

free radical (Initiation), chain porpgation (propogates) and termination via terminator

28
Q

condensation polymer reaction

A

a difunctional group is added to make either polyesters or polyamides following reaction and can keep going but will stop when a singular is added to the compound

29
Q

natural polymers

A

silk, cotton, wool, linen, cellulose

30
Q

synthetic polymers

A

plastic, nylon, ryon, polyester

31
Q

polymerization

A

the process of chain reactions by which monomers are linked together to form a polymer

32
Q

cross linkage

A

polymers which are unstaurated are attracted to one another via intemroleculer attraction between polymers and there form interlocking bond like a net between polymers making the structure strong, rigid and inflexible

33
Q

properties of polymers

A

unreactive - unsaturated alkanes
mouldable / flexible - weak intermolecular foces, np
strength - degree of cross linkage
diff side groups make diff properties