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
Preparation u Alcohols when heated in presence of H2SO4‚ H3PO4‚ P2O5‚ Al2O3 or BF3 undergo loss of water molecule with the formation of alkene. Conc. H2SO4 180oC H3PO4/P2O5 200oC Al2O3/BF3 350oC CH3-CH=CH2 + H2O CH3-CH2-CH2-OH CH3-CH=CH2 + H2O CH3-CH=CH2 + H2O u u Mechanism: In the first step OH group of the alcohol is protonated in a fast reversible reaction. Unlike OH group‚ protonated OH group is a good leaving group. Step 1: CH3 CH3-C-CH3 + H+ HO CH3 CH3-C-CH3 H2O+
Premium Alcohol Alkene
Experiment 23: Synthesis of an Alkene April 5‚ 2013 Purpose: Results and Discussion The weight of our n-Butyl Bromide sample (actual yield) was 0.09g. The percent yield was found to be 4.38%. Only 0.09g of the theoretical 2.055g yield was obtained. The boiling point was 104° C‚ which is higher than the literature value of 101° C. This is due to the sample being somewhat impure‚ as impurities tend to increase boiling point. When IR spectroscopy was performed‚ there were no OH stretches
Premium Water Yield Distillation
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
to the carbon chain than alkanes. Are alkenes with double bonds. Are alkynes with triple bonds. 1 Structure of Alkenes Alkenes (and alkynes) are unsaturated hydrocarbons Alkenes have one or more double bonds The two bonds in a double bond are different: - one bond is a sigma () bond; these are cylindrical in shape and are very strong - the other is a pi (π) bond; these involve sideways overlap of p-orbitals and are weaker than bonds Alkenes are flat and have a trigonal planar shape
Free Benzene Hydrocarbon Alkene
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
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
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
Old Dominion University ORGANIC 214 Alkene Addition Submitted by: Alkene addition: Bromination of (E) Stilbene Introduction: In this lab we used the greener approach‚ which involves the addition of bromine across a double bond. When bromine reacts with E-stilbene (trans-1‚2-diphenylethene)‚ two new chiral carbons are created from the sp2 carbons‚ therefore 3 different dibrominated stereoisomers are possible: meso-(1R‚2S)‚ or the raceminc mixture-(1R‚2R) or (1S‚2S)-dibromo-1‚2-diphenylethane
Premium Carbon Melting point Stoichiometry
presence in an organic molecule. Common functional groups found in organic molecules are listed below: * Alkene * Primary alcohol * Tertiary alcohol * Aldehyde * Ketone * Carboxylic acid * Ester * Halogen alkane * Phenol Alkene In organic chemistry‚ an alkene is an unsaturated chemical compound. This means it contains a carbon – carbon bond. All alkenes are hydrocarbons‚ (a molecule made of carbon and hydrogen atoms)‚ and can only form one double bond which must
Premium Alcohol Functional group Carboxylic acid