alchols Flashcards
alchols are produced industrailly by
hydration of alkenes in the presences of acid catalyst (H3PO4)
ethanol is produced industrially by … and why
fermentation of glucose
cheaper than hydration as carried out at lower temp but has to be done in batches so slower process with a lower % yield
glucose –> ethanol + carbon dioxide
yeast must be present
how is biofuel formed and why is it used
separating of ethanol by fractional distillation. it is said to be carbon nuetral as the carbon given out when burned is equal to the carbon taken in by crops during the growing phase
environmental issues linked to biofuels use
destruction of crops
transportation of crops
classification of alchols
primary - carbon bonded to OH is bonded to one other C
secondary - carbon bonded to OH is bonded to 2 other C
teritary - carbon bonded to OH is bonded to 3 other C
oxidation of primary alcohols
forms aldehydes
reagent: acidified potassium dichromate [O]
conditions: heat under distillation
oxidation of aldehyde
forms carboxyllic acid
reagent :acidified potassium dichromate [O]
conditition: heat under reflux
oxidation of secondary alchols
forms ketones
reagent: acidified pottasium dichromate
condistion : heat under reflux or distillation
primary alchol -> carboxylic acid
oxidation
reagent : acidified potassium dichromate[O]
condition: heat under reflux, excess oxidising agent
oxidation of tertiary alchols
cannot be easily oxisied
explain how the method used to oxide a primary alcohol determines what the product obtained is
under distillation so aldehydes not mixed back into oxidising agent instead separated to prevent further reaction to carboxylic acid that would take place if under reflux
observation of colour change when alchol oxidised
orange –> green
chemical test to distinguise between aldehydes and ketones
fehlings solutiuon
aldheyde : brick red precicitate
ketone: NVC
tollens reagent
aldehyde: silver mirror forms
ketone: NVC
alchol –> alkene
elimination
catalyst : hot conc H2SO4 OR AlO3
condition: 600K
lone pair on O in R-OH attracted to &+ on H causing R-OH2 where O is +, C-O is broken removing water resulting in C-C+ electrons from C-H to C-C+ forming C=C and H+
H+ reformed therefore catalyst
importanct of alchol-> alkene elimination reaction
means addition polymers can be produced from fermentation without need for crude oil( a non-renewable resource)