Experiment 4 Preparation of Isoamyl acetate. H 2 SO 4 + H 2 O.

Slides:



Advertisements
Similar presentations
Preparation of N,N-Diethyl-m-toluamide
Advertisements

Gravimetric Analysis.
Synthesis of Lidocaine (Step 3)
Contact process KING OF CHEMICAL. What is it It is the method to produce high concentration of sulfuric acid for industrial needs.
Preparation of a haloalkane. Haloalkanes can be made by a substitution reaction with an alcohol. Tertiary alcohols are the most reactive, and therefore.
Lecture 11a Esterification. Introduction Esters can be obtained by a broad variety of reactions Acyl chloride Accessibility of SOCl 2 Anhydride Availability.
Experiment 18: THE GRIGNARD REACTION Objectives:  To synthesize a 3 o alcohol from an alkyl halide and a ketone using a Grignard reaction.  To purify.
Identification of an Unknown Oxygen-Containing Compound
Chemistry 2412L Esterification pre-lab lecture. Properties of Esters The purpose of this lab is to study the chemical properties of esters Esters are.
Bromobutane. Halogenoalkanes Halogenoalkanes are hydrocarbon chains that have one or more hydrogen atom(s) exchanged for halogen atom(s).
Synthesis of Isopentyl (Amyl) Acetate Ester (Banana Oil)
DISTILLATION Imelyn will show you how to set up for distillation. Scroll down.
Sea water BLOWING OUT TOWER STEAMING OUT TOWER CONDENSER SEPARATOR DRYER.
Distillation – A Way of Life Zach Alison. What is distillation? The process of heating a liquid until it boils, capturing and cooling the resultant vapors,
Dehydration Expt. – GC Results
AL CHEM REVIEW ORGANIC CHEMISTRY. AL CHEM Written Practical [Organic Chemistry] p.1 ~ Organic Synthesis ~ Organic Acid separate How to separate the product.
Method 3: Simple Distillation
ESTERS: SYNTHESIS AND FRAGRANCE
Midterm Review for Organic I lab
Experiment 18: THE GRIGNARD REACTION.
Experiment 18: THE GRIGNARD REACTION Objectives:  To synthesize a 3 o alcohol from an alkyl halide and a ketone using a Grignard reaction.  To purify.
Organic Chemistry Lab II, Fall 2009
ACID-CATALYZED DEHYDRATION OF AN ALCOHOL WITH REARRANGEMENT
Experiment 21: ESTERS: SYNTHESIS AND FRAGRANCE Objectives:  To synthesize an ester from acetic acid with isoamyl alcohol under reflux.  To purify your.
Do now! Can you read through the notes we made last lesson?
2f Sulphur and Nitrogen.
SALUTATION. PREPARATION OF UREA-FORMALDEHYDE RESIN.
Organic Chemistry Lab 318 Spring, DUE DATES Today –Aldehyde/Ketone Qualitative Analysis Report at beginning of lab –At end of lab -- copy of laboratory.
Science Jeopardy ABCDE Final Jeopardy.
Buffers and K a ’s. What are Buffers? At times, it is essential to maintain a certain pH. At times, it is essential to maintain a certain pH. To achieve.
Separating a Synthetic Pain Relief Mixture
Heating Curves. Energy and Phase Change When adding heat to a solid, energy added increases the temperature and entropy until the melting point is reached.
Dehydration of 2-methylcyclohexanol -- an E 1 reaction.
Water is made up of molecules. Water changes state (gas, liquid, solid) when it’s molecules are heated or cooled.
SALTS When you hear the word salt, what do you think of?
Lab Activity 4 A. Extraction & Determination of Crude Fat from Plant or Animal Tissues B. Determination of Dry Matter and Moisture Content In Plant Materials.
Crystallization is a separation technique that is used to separate a solid (SOLUTE) that has dissolved in a liquid (SOLVENT) and made a solution (homogenous.
1. What is a thin blanket of air that surrounds the Earth?
Experiment 6: EXTRACTION of ANALGESICS. Objectives  To learn the techniques of acid-base extraction, drying organic solvents, and vacuum filtration.
PROBLEMS CH 16. Learning Check Give the IUPAC and common names for the following. A. B. C.
Topic 17 Equilibrium Liquid-vapour equilibrium The equilibrium law.
Experiment 18: THE GRIGNARD REACTION Objectives:  To synthesize a 3 o alcohol from an alkyl halide and a ketone using a Grignard reaction.  To purify.
By: Chanelle Grannum. Distillation is the process of heating a liquid until it boils, capturing and cooling the resultant hot vapors, and collecting the.
Dehydration of 2-methylcyclohexanol -- an E 1 reaction.
Change of Phase Chapter 23. Topics  Phases  Evaporation  Condensation  Evaporation & condensation rates  Boiling  Freezing  Energy & changes of.
Oxidation of Cyclododecanol
(2-chloro-2-methylpropane) Preparation of t-butyl chloride.
Pavia Experiment 14a Starting materials – Solubility, ionization, LD 50 Product properties – Solubility, boiling point, ionization Reactions – Overall.
Complete the table NameFormulaStructure+ O 2 Miscibility in water methaneCH 4 CO 2 + H 2 OImmiscible ethaneC2H6C2H6 CO 2 + H 2 OImmiscible propaneC3H8C3H8.
Distillation!  By Chantalle and Sharnhi.
ACIDS AND BASES. Every liquid will probably have some acidic or basic traits. Water can be acidic or basic in different reactions. Water can even react.
Planning a synthesis. Retrosynthesis involves working backwards from a target molecule to determine suitable starting materials for its preparation.
Mixtures.
Distillation First the mixture is heated up.
Preparation of Methyl Benzoate
Corn Mash and Distillation
REFLUX Dan will show you how to set up a reaction under refluxing conditions. Scroll down.
Chapter 7 Quiz.
Preparation of t-butyl chloride
Preparation of t-butyl chloride
Solutions.
PROBLEMS CH 16.
Brooke Conrad Du$tyyyyyyyy
Reaction time زمن الرجع.
Preparation of t-butyl chloride
Synthesis of Banana Oil
Preparation of t-butyl chloride
Distillation.
Ethanoic acid test.
Presentation transcript:

Experiment 4 Preparation of Isoamyl acetate

H 2 SO 4 + H 2 O

120 V H 2 O in H 2 O out Variac condenser heating mantle set Variac to ≈ 75% of line voltage clamp ring clamp

1.The reaction is heated to reflux 2.After 1 hour the reaction is cooled and water is added; the layers are separated and the organic layer is washed with NaHCO 3 and separated. 3.The organic layer is dried over anhydrous MgSO 4 or anhydrous Na 2 SO 4. 4.The organic layer is distilled.

1.Why do you heat the reaction? Reaction rate doubles for an increase in 10 °C. 2.Why do you use an excess of acetic acid? 3. Why do you wash with NaHCO 3 ? 4.Why do you dry the isoamyl acetate? The presence of water affects the distillation. 5.Why do you distill the isoamyl acetate? Distillation is an important way in which liquids are purified. Forces the equilibrium to the right. To neutralize the xs acetic acid and any H 2 SO 4 present.

Simple Distillation open to the air