3-Dihydropthalazine Lab Report

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Abstract: Luminol, known for it’s use in crime labs to identify blood, was one of the main components used in the experiment which sought to use a starting material, convert it to a product, and then use the product as the starting material for an alternate reaction. In the experiment conducted in lab, 5-nitro-2,3-dihydropthalazine-1,4-dione was used as starting material, and when the nitro group was added to sodium hydrosulfite in 3M sodium hydroxide in water it was reduced and the resulting amine was used as a starting material to investigate properties of luminol. Chemiluminescence’s release of glowing light was due to the breaking of bonds brought upon by the excitation of electrons to release energy, and this resulting glow produced is …show more content…

After the solution was stirred, the solution turned into a mustard yellow color. When the luminol was dissolved into NaOH the solution turns a dark brown color. After the water was added into stock solution A, the color appeared medium brown. Following this, after the potassium ferrycyanide and hydrogen peroxide were mixed, stock solution B was made and appeared a yellow color. When stock solution B was diluted with water the resulting solution B appeared a to be a light yellow. Finally, after diluted solution A was added to solution B in a dark room the appearance of the solution was a glowing blue …show more content…

What is the difference between chemiluminescence and fluorescence? Where does the ENERGY for light emission come from in each case?
Chemiluminescence was used to chemically excite a molecule which caused it to fall back down to the ground state causing released energy. Fluorescence usually occurs when light is absorbed from an alternate basis. Fluorescence usually occurs when its energy from external means obtains energy and alternatively chemiluminescence obtains its energy from chemical means.
6. In the chemiluminescence reaction, a diene is generated on the luminol molecule. Why does the reaction not progress from that point forward as a Diels-Alder reaction with molecular oxygen acting as a dienophile? How does ground-state molecular oxygen exist and does this affect the possibility of a Diels-Alder mechanism with O2?
The reaction does not progress because in a triplet state oxygen is a diradical and a Diels Alder usually necessitates a double bond in singlet state.4 Diels Alder does not occur due to oxygen being being a diradical due to a non sufficient amount of electrons to make two sigma bonds on

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