Preparation and Characterization of Alkene Balacanao‚ Gladys A.1‚ Miranda‚ MarilynI2 1 Student (s)‚ Subject/Section‚ School of Chemical Engineering‚ Chemistry and Biotechnology‚ Mapua Institute of Technology; 2 Professor‚ School of Chemical Engineering‚ Chemistry and Biotechnology‚ Mapua Institute of Technology [pic] ABSTRACT The purpose of this experiment is to prepare cyclohexene form cyclohexanol‚ and know the properties of alkene. The first part of this experiment is preparation of cyclohexene
Premium Sulfuric acid Distillation Alkene
Bromination of Trans-Cinnamic Acid Christopher B. Martin CHEM 3411 1 Mechanism of Bromine Addition to Alkenes Understanding the chemical mechanism (order of bonds broken and made as well as intermediates formed) has a great value in chemical synthesis. The chemical mechanism of a reaction will influence the rate of the reaction‚ the stereochemistry of the product(s)‚ and the extent of possible undesired side reactions. Organic reaction mechanisms investigate the path towards a desired product
Premium Chemistry Chemical reaction Organic reaction
Exercise 5 Comparing the Reaction Rates of Alkanes and Alkenes Group # 4 Members: Pangan‚ Sam Margarette Perales‚ Angelica Ibay‚ Sophia Irigan‚ Sharien May Sorensen‚ John Antonio Ocan‚ Emmanuel Submitted to: Ms. Ginalyn Cuenca Mr. Neil Abreo Date: December 6‚ 2012 Introduction Alkanes are hydrocarbons with only single bonds between the atoms. Saturated hydrocarbon is the other term for it. They are used as fuels because they are non-reactive and also do not conduct electricity
Premium Fat Saturated fat Fatty acid
Comparing alkanes and alkenes Aim: Is cyclohexane more or less reactive than cyclohexene in the presence or absence of light Hypothesis The cyclohexene will reactive the fastest because being an "ene" it has a electron rich area making it more reactive than cyclohexane but neither one of the will react without light Materials * 4x 250ml conical flasks * 2 rubber stoppers * Aluminium foil * Cyclohexane * Cyclohexene * Bromide water * Measuring cylinder
Premium Erlenmeyer flask Oxygen Color
Abstract The bromination of trans-cinnamic acid was completed to determine dibromide’s stereochemical structure and its mechanism. After the addition of bromine to trans-cinnamic acid‚ the product was identified by its melting point and infrared spectrum resulting in erythro-2‚3-Dibromo-3-phenylpropanoic acid after comparing similar properties. Introduction In this lab‚ the bromination of trans-cinnamic acid was completed to determine dibromide’s stereochemical structure‚ and from there determine
Premium Solvent Acetic acid Ethanol
Notes Aldehydes and Ketones The major similarity between an aldehyde and a ketone is the carbonyl group. A carbonyl group is a carbon atom doubly bonded to an oxygen atom. [pic] Both molecules have a carbonyl group‚ the difference the number of carbons bonded to the carbonyl carbon. An aldehyde will have none or one and a ketone will have two carbons. All aldehydes‚ except formaldehyde‚ will have a hydrogen atom on one side of the carbonyl carbon and at least on carbon on the other side
Premium Oxygen Alcohol Carbonyl
Alkene Synthesis from Alcohol: Preparation of Cyclohexene From Cyclohexanol 5/29/14 Abstract: A 42.89% yield cyclohexene was successfully synthesized from 10.0 mL cyclohexanol by unimolecular elimination (E1) through the dehydration of cyclohexanol and confirmed via a bromine test and the IR spectra. Introduction: Alkenes are hydrocarbons that have carbon–carbon double bonds and are one of the many functional groups in organic molecules. Alkenes are sp2 hybridized
Premium Alkene Alcohol Oxygen
Alkane‚ Alkene‚ Alkyne & Aromatic Learning Objectives 1. 2. 3. Determine the IUPAC name‚ common name and structure of an alkanes‚ alkenes and cycloalkanes. Identify the physical properties of alkanes. Describe briefly natural sources and importance of alkanes Describe reactions of alkanes Propose a mechanism on free radicals substitution 4. 5. 6. Describe the preparation and reactions of alkenes. 7. Propose mechanism on preparation; dehydration of alcohol 8. Define carbocation
Premium Hydrogen Benzene Methane
SYNT 0719 – Brominating Alkenes OBJECTIVE The purpose of this lab will be to brominate trans-stilbene by using acetic acid and pyrimidium tribromide by refluxing the mixture. To test the purity of product I will take the melting point which should be around 240 ºC along with a flame test which should be green-blue. CHEMICAL PROPERTIES TABLE See Attached Lab Notebook Copies REACTION MECHANISM In this lab we used multiple techniques to complete and verify the bromination of trans-stilbene. First
Premium Distillation Acetic acid Oxygen
free-radical chain bromination‚ we were expected to be able to determine the relative reactivates of the many types of hydrogen atoms involved toward bromine atoms. Bromination is defined to be a regioselective reaction meaning bromine has preference of making or breaking a bond over all other directions that it may have had available. In this case‚ Markovnikov’s rule is revealed to be the case in this situation that states that adding a protic acid represented as HX to an alkene (sp2 hybridized)‚
Premium Chemistry Acid Oxygen