Bunsen Burners

Burner, Bunsen Burner, ring P. 48 Burner, wingtop Casserole, 150 cc. P. 48, 52, 55 Casserole, 750 cc. P. 1, 55 Clamp, burette, small Clamp, test tube holder... 

Air line 1 Beaker, 10 mL 1 Beaker, 50 mL 1 Beaker, 100 mL 1 Bottom, burner 1 Box, fluorescence viewing 1 Bulb, pipet, 2 mL 1 Burner, Bunsen... 

Balance, 0.0 Ig Blade, razor, single edge Brush, test tube Burner, Bunsen Clamp, buret... 

Using the new burner, Bunsen and Kirchhoff were able to clearly see the spectra of all the chemicals they were studying. Together, they catalogued the spectra of all the known elements. This aided chemists enormously, because by identifying their spectral patterns, chemists conld determine the composition of any unknown substance. In the process of cataloguing the spectra of the elements, Bunsen and Kirchhoff discovered two new elements that they named after the colors of their spectral lines cesium (blue) and mbidium (red). Using Bunsen and KirchhofPs new analytical technique and the spectroscope they next developed, many new elements were subsequently discovered. But spectroscopy not only opened the door to the further analysis of earthly substances, the composition of the stars could also now be deduced. 

The material to be steam-distilled (mixed with some water if a solid compound, but not otherwise) is placed in C, and a vigorous current of steam blown in from D. The mixture in C is thus rapidly heated, and the vapour of the organic compound mixed with steam passes over and is condensed in E. For distillations on a small scale it is not necessary to heat C if, however, the flask C contains a large volume of material or material which requires prolonged distillation, it should be heated by a Bunsen burner, otherwise the steady condensation of steam in C will produce too great a volume of liquid. 

A skilled worker can use a micro-Bunsen burner for most types of heating. Nevertheless, as there is a tendency for a liquid to shoot out of a small test tube when heated, it is preferable to place the tube in a hot water-bath or in a metal heating block. A small glycerol bath is suitable for distillations and heating under reflux, the glycerol being subsequently easily removed from flasks, etc., by washing with water. 

The heating of the vessels is accomplished by means of a small bath or a micro-Bunsen burner. The vessel can be clamped at such a distance from the burner that the contained liquid boils gently under reflux. Smooth boiling is ensured by the addition of 1-2 minute pieces of unglazed porcelain, or of a short piece of melting-point tubing open at both ends. 

If the solid does not dissolve in the cold solvent gently heat the mixture over a micro-Bunsen burner or in a small water-ba until the liquid boils. Continue to add o-i ml. portions of solvent until the solid dissolves. [If more than about i ml. of solvent is required, the solvent is considered unsatisfactory.] If a clear solution is obtained, cool the tube and scratch it below the surface of the solution with a very fine glass rod and proceed as suggested on p. 16. In general, the products from the choice of solvent investigation are not discarded but added to the main bulk of the crude product for recrystallisation. 

The liquid becomes progressively darker in colour, and then effervesces gently as ethylene is evolved. Allow the gas to escape from the delivery-tube in T for several minutes in order to sweep out the air in F and B. Now fill a test-tube with water, close it with the finger, and invert the tube in the water in T over the delivery-tube so that a sample of the gas collects in the tube. Close the tube again with the finger, and then light the gas at a Bunsen burner at a safe distance from the apparatus. If the tube contains pure ethylene, the latter burns with a clear pale blue (almost invisible) flame if the ethylene still contains air, the mixture in the test-tube ignites with a sharp report. Allow the... 

When the reaction is complete, heat the stirred mixture carefully under reflux over a Bunsen burner and asbestos gauze for I hour if the mixture becomes too thick for efficient stirring, add up to 15 mL of acetic acid. Now decant the hot mixture into 500 ml. of vigorously-stirred ice-cold water wash the residual zinc thoroughly with glacial acetic acid (2 portions each of I -2 ml.), decanting the acid also into the stirred water. 

A beaker is placed under Y and the combustion may now be started. The Bunsen burner, with the air-hole wide open, and the... 

During this process some water will have condensed in the steam-trap D and also in the distillation bulb F. If at the end of the steaming-out process, the Bunsen burner is removed from the generator A, the pressure in A will be reduced owing to steam condensation, and the liquid in F will be sucked back into D provided that the benL-over tube is carefully adjusted, the bulb F may be almost completely emptied of liquid as desired. Finally the condensed water in the steam-trap D may be run out by op ing the tap Tj. 

Prepare a coil of copper wire by winding several turns around a glass tube. Heat the coil in the oxidising flame of a Bunsen burner for 1-2 minutes and plunge the spiral, whilst still red hot, into a test-tube containing a solution of 1 ml. of methyl alcohol and 5 ml. of water. Stopper the test-tube loosely, cool, remove the wire, and repeat the process two or three times. Observe the odour of the solution and use it (or formalin diluted with water) to carry out the following tests. 

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