Your Status: Logged out Log in

Compare the rate of hydrolysis of some halogeno-compounds.  

Member rating: No Rating | Words: | Submitted: Fri Jan 30 2004

Page Preview
Preview
Previous 1 of 5 Next

On the left is an image preview of every page of this document, and below are the first 150 words with formatting removed:

Carmen Tse 7C 21 Chemistry Experiment No.19 Comparison of Rates of Hydrolysis of Halogeno-compounds Objective To compare the rate of hydrolysis of some halogeno-compounds. Introduction Halogeno-compounds are organic compounds composed of carbon, hydrogen and halogen. One of the characteristic reactions of haloalkanes is nucleophilic substitution reactions: Nu- + R-X --> R-Nu + X- In the above experiment, the nucleophile is H2O. OH- attacks the electropositive carbon centre and displaces a halide ion from the haloalkane. This kind of substitution is called hydrolysis. The halide ions substituted can be identified by silver nitrate solution. Ag+ (aq) + X- (aq) --> AgX (s) where X is the halide ions The overall equation is: OH- + R-X + Ag+ --> R-OH + AgX In this experiment, the rates of hydrolysis of halogeno-compounds are compared in 3 categories: 1. chloro-, bromo-, and iodoalkanes; 2. primary, secondary and tertiary haloalkanes; 3. haloalkane, halobenzene and (halomethyl)benzene Chemicals Ethanol about 20cm3 0.1M silver nitrate 10cm3 1-chlorobutane 5drops 1-bromobutane 15drops 1-iodobutane 5drops 2-bromobutane 5drops 2-bromo-2-methylpropane 5drops Bromobenzene 5drops Precaution Ethanol is volatile. It easily...

Get instant access



  • Instant, unlimited access to our documents in full
  • Swap your work for free access, or pay £4.99
  • To see the full version of this document and 151,744 others
Register Now