Synthesis of Divanillin Lab Report Essay Example

Synthesis of Divanillin Lab Report Paper The dimmer bond forms between two carbons that have each lost an electron and have one to share, The dimmer bond does not involve an oxygen, so this is called oxidative demarcation because two identical compounds are bonded at oxidized carbons. 2) Draw resonance structures for the phenotype anion: 3) Why does the dimmer bond form between the #5 Carbons? A. When the hydrogen peroxide reacts with the peroxides, 2 equivalents of a hydroxyl free radical are formed. Those free radicals take a hydrogen (including its electron) from the vanilla molecules, forming phenol free radicals. The cost stable location for the resonating electron on this free radical is on the number 5 carbon (Roth to the phenol). The resonating electrons on each vanilla free radical form a covalent bond, forming the dimmer. 4) Why is this green Chemistry? A. Green Chemistry, simply put, avoids the use and creation of toxins and waste that harms the environment. Green chemistry seeks to stop pollution from chemical production and to use fewer natural resources. This experiment is green chemistry because the reactants used and the products are all non-toxic ND sate tort the environment. In specific, this experiment involves one of the Green Chemistry developments Rye ¶j Noir made in the use of hydrogen peroxide for clean oxidations. The hydrogen peroxide in this experiment does not produce toxic waste like heavy metal oxidants do; it only produces water. We will write a custom essay sample on Synthesis of Divanillin Lab Report specifically for you for only $16.38 $13.9/page Order now We will write a custom essay sample on Synthesis of Divanillin Lab Report specifically for you FOR ONLY $16.38 $13.9/page Hire Writer We will write a custom essay sample on Synthesis of Divanillin Lab Report specifically for you FOR ONLY $16.38 $13.9/page Hire Writer