Zusammenfassung der Ressource
organic chemistry
- combustion
- alcohol+O2->CO2+H2O
- biofuels(more photosynthesis)
- alkane
- complete(o2 not limited)
- alkane+O2->CO2+H2O
- O2 limited (incoplete )
- alkane+O2->CO2+CO+H2O
- elimination
Anmerkungen:
- a reaction in which a small molecule, such as H2O or HCl, is removed from an organic molecule
- of Halogenoalkanes
- removed molecule is HX
- ethanolic NaOH
- OHminus act as base
- The original 2-bromopropane molecule has lost an H atom and a Br atom. We can think of it as HBr
being eliminated from the halogenoalkane. The ethanolic OH– ion acts as a base, accepting an H+
from the halogenoalkane to form water. The C Br bond breaks heterolytically, forming a Br– ion and
leaving an alkene as the organic product
- dehydration of alchols
- H2O is removed
- alkene+water
- alcohol vapor
- Al2O3 or SiO2or H2SO4
- substitution
Anmerkungen:
- eaction that involves the replacement of one atom, or group of atoms, by another.
- ree-radical substitution the reaction in which halogen atoms substitute for hydrogen atoms in alkanes. The mechanism involves steps in which reactive free radicals are produced (initiation), regenerated (propagation) and consumed (termination)
- Alkanes(free radical substitution
- homolytic fission
- mechanism
- termination
- only free radicle react
- they form a molecule
- propagation
- free radicles are very reaxtive
- free radicles hits the normal molecule >CH3radicle
- intiation
- energy is put in to break
the bonds,
- only 2 free
radicles formed
- halogenoalkane
- with alkali(OHminus)Aq
Anmerkungen:
- The halogen atom in the halogenoalkane
is replaced by an OH, hydroxyl group, so the organic
product formed is an alcohol
- gives alcohol
- wtih cyanide ion,CN- in ethanol
- heated in reflux with the halogenoalkane
- extra carbon atom is added
- CH3CH2Br + CN->CH3CH2CN + Br–
- with NH3
- If a halogenoalkane is heated
with an excess of ammonia
dissolved in ethanol under
pressure, an amine is formed.
- CH3CH2Br + NH3--> CH3CH2NH2 + HBr
- amine is formed
- Mechanism of nucleophilic substitution
in halogenoalkanes
Anmerkungen:
- nucleophiles are donors of an electron pair and
are attracted to electron-deficient atoms
- primary SN2(heterolytic)
- when C is boned to X and one CH3(+2H)
- SN1 Tertiary
Anmerkungen:
- The Br– ion forms again, as in the SN2 mechanism,
but in this mechanism a carbocation ion forms. This
does not happen with primary halogenoalkanes. This
is because tertiary carbocations are more stable than
primary carbocations due to the inductive effect of the
alkyl groups attached to the carbon atom bonded to
the halogen. Alkyl groups tend to release electrons
to atoms attached to them. So a tertiary carbocation
has three alkyl groups donating electrons towards the
positively charged carbon atom, reducing its charge
density. This makes it more stable than a primary
carbocation, which just has one alkyl group releasing
electrons
- the C bonded to X is also bonded to 3C(s) or CH3(s)
- of alcohols forms halogenoalkanes
- hydrolysis
Anmerkungen:
- the breakdown of a compound by water, which is often speeded up by reacting with acid or alkali.
- nucleophilic hydrolysis of halogenoalkane
- CH3CH2Br+H2O(IN AgNO3)-->CH3CH2OH+H-PLUS+Br MINUS
- reflux
- oxidation
Anmerkungen:
- crease in Oxidation nu#
losss of e
gain of oxygen
loss of hydrogen
- alkene
- alkene converted to diol
- cold
- dilute acidified KMnO4
- CO2 or aldehyde.carboxylic and or keton
- hot
- conc. MNslo
- reduction
Anmerkungen:
- decrease in Oxidation nu#
losss of e
gain of oxygen
loss of hydrogen
- Addition
Anmerkungen:
- an organic reaction in which two
reactant molecules combine to give a single
product molecule.
- c=c broken and eache carbon makes a new segma bond
- alkene[C=C is broken]
- H2->>alkane
- Ni(finely powdered catalyst
- 140 degree C
- steam->> alcohol
- gaseous alkene
- 6mega pa
- 330 degree C
- catalyst
- phosphoric
- tungestic
- dilute H2SO4
- mechanism of electrophilic
- HX->> halogenoalkane
- conc.sol. of HX(HF,HCl... ROOM TEP
- when not symetric ^ markovnikov alkene will decolorise
Anmerkungen:
- When a compound HX is added to an unsymmetrical alkene, the hydrogen becomes attached to the carbon with the most hydrogens attached to it already.
- electrophile can easily attact the c=c
Anmerkungen:
- electrophile acceptor of e
H+
- HX is polar due to electronegativity
- the only difference is in how fast the reactions happen with the different hydrogen halides. The rate
of reaction increases as you go from HF to HCl to HBr to HI.
Anmerkungen:
- The reason for this is that as the halogen atoms get bigger, the strength of the hydrogen-halogen bond falls. Bond strengths (measured in kilojoules per mole) are:
H-F
568
H-Cl
432
H-Br
366
H-I
298
- c=c will polarize the nonpolar br-br
Anmerkungen:
- Bromine as an electrophileThe bromine is a very "polarisable" molecule and the approaching pi bond in the ethene induces a dipole in the bromine molecule. If you draw this mechanism in an exam, write the words "induced dipole" next to the bromine molecule - to show that you understand what's going on.
- X2(halogens)
- yellow color of br is decolorised
- polymerizzation