A Greener Bromination Of Stilbene

BROMINATION OF TRANS – STILBENE

AIM:

The aim of this experiment is to carry out an addition reaction using trans-stilbene and bromine reagent to produce 1,ii-dibromo-1,2-diphenylethane. Every bit well-nigh chemicals used in this experiment are toxic / harmful, PPE must be used throughout and the experiment should be carried out inside a smoke hood.

THEORY:

Bromine and chlorine readily undergo addition reactions with alkenes. This practical involves the bromination of trans-stilbene using a 10% bromine dichloromethane solution. Hence, an addition reaction takes identify an 1,2-dibromo-1,two-diphenylethane is formed.

MECHANSIM: The alkene, trans-stilbene, acts as a nucleophile and the bromine acts as an electrophile. Hence, the nucleophilic double bond undergoes an electrophilic addition reaction by the bromine reagent. The Br–Br bond becomes polarized and the more positively charged Br atom is transferred to the alkene to yield a bromonium ion. The improver of bromine begins at one side of the double bond (either side is equally likely, but only 1 choice is drawn) and is followed by set on of bromide ion on the bromonium ion (over again, attack could occur at either carbon since the ion is symmetric, but only 1 selection is drawn). The result is a trans dibromide, as shown above.

The production of this reaction, one,ii-dibromo-1,ii-diphenylethane, has two stereogenic

centres which normally leads to predict four (2n= 22 in this case) possible

stereoisomers (i.east. four optical isomers). However, there are only 3 possible isomers in the case of 1,2-dibromo-1,2-diphenylethane since i, the then-chosen meso isomer, is superimposable on its mirror image.

PROCEDURE:

• 5g of trans-stilbene were added to a 250cm^three conical flask, followed by 40cm³ of dichloromethane. The flask was swirled to dissolve all the stilbene.
• Approximately 15cm³ of ten% bromine-dichloromethane solution were advisedly measured.
• 5cm³ of the bromine solution were added to the solution of stilbene and contents were swirled until the reddish chocolate-brown colour of the bromine solution disappeared.
• A further 5 cm³ of the bromine solution were added to the solution of stilbene and the contents were swirled over again until the reddish brown colour of the bromine solution disappeared for a second fourth dimension.
• The remaining bromine solution was added and the mixture was swirled for several minutes to ensure bromine's colour persisted.
• Cyclohexene was added driblet wise to the flask until the bromine color disappeared.
• The flask was so cooled in an ice bath and the crystals were nerveless after carrying out filtration using a Buchner funnel and flask.
• The crystals were washed with 15cm^three common cold dichloromethane and were allowed to dry.
• The melting point of the product was determined.

RESULTS AND CALCULATIONS:

Experimental data was recorded in the following tables:

Discussion:

SOURCES OF ERRORS:

• When transferring 5g of trans-stilbene to the conical flask, at that place was still some trans-stilbene left on the weigh boat. (Systematic Fault)
• More crystals would have been formed and a meliorate pct yield could have been obtained if the flask was left in the water ice bath for a flake longer. (Systematic Mistake)
• All the crystals were not transferred from the Buchner funnel to the petri dish. (Systematic Mistake)

CONCLUSION:

Trans-stilbene was brominated and 5.67g of 1,ii-dibrmono-ane,ii-diphenylethane were obtained. This is a pct yield of 60.07%. The melting point range of 1,two-dibromo-one,2-diphenylethane was institute to be 240.2^o to 241.7^o C.

REFERENCES:

• http://fscimage.fishersci.com/msds/58466.htm for literature value of ane,2-dibromo-1,2-diphenylethane (i.e. melting point = 241^o C)
• Google images for structural equation of the reaction.

A Greener Bromination Of Stilbene,

Source: https://www.odinity.com/bromination-of-trans-stilbene/

Posted by: freemanyouripasted.blogspot.com

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