Experiment Six: Synthesis of Bromohydrin – Flashcards

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question
What are we adding to the C=C in this reaction?
answer
OH and Br
question
what does it mean that the OH adds Markovnikov?
answer
the OH adds to the more substituted side
question
what does it mean to say that Br adds anti-markovnikov?
answer
the Br adds to the less substituted side
question
What type of stereoselectivity occurs in addition of Br and OH?
answer
anti OH is 180 degrees away from Br
question
What acts as the electrophile?
answer
halogen
question
what acts as the nucleophile?
answer
water
question
What is our source of Br?
answer
NBS N-Bromosuccinimide easy to handle, solid electrophile source
question
What is the difference between adding Br and OH syn or anti?
answer
steric interactions and very different chemical properties
question
What are our reactants?
answer
1-methylcyclohexene (liquid) water (co-solvent) (liquid) THF (co-solvent) (liquid) NBS (solid)
question
What is added last in the reactant mixture?
answer
liquid 1-methylcyclohexene
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What is the intital color of the reactant mixture?
answer
yellow due to unreacted Br
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what is the ending color of the reaction mixture?
answer
clear due to the fact that all the Br is reacted
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How do we quench the reaction following the color change?
answer
add water
question
How do we extract the organic layer from the aqueous layer?
answer
place it test tube and use pipet to trasfer bottom organic layer to new test tube
question
what does the organic layer contain?
answer
1-methyl-2-bromocyclohexanol (product) and the succinimide byproduct THF and H2O solvent
question
How do we remove water from organic layer?
answer
using magnesium sulfate drying agent
question
How do we separate succinimide byproduct from product?
answer
using chromatographic purification
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what is the purpose of chromatographic purification?
answer
to separate organic molecules of different polarity
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what medium is used for chromatographic purification?
answer
silica gel
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how does chromatographic purification work?
answer
the polar OH bonds on the surface of the silica gel attract the polar succinimide by product to the surface and prevent passage cyclohexonal is nonpolar and can pass through
question
How do we proceed with chromatographic purification?
answer
prepare chromatographic column with silica gel, then use pipet to transfer organic layer into column rinse test tube with dicholormethane and transfer remaining organic layer add dicholormethan to column use pipet bulb to push cyclohexanol and dicholormethane through the silica gel
question
How do we remove the dicholormethane?
answer
rotary evaporation
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what should the product look like after rotary evaporation?
answer
colorless liquid
question
what are we looking for in the IR spectrum for this experiment?
answer
the absence of C=C and the presence of C-OH
question
What is the beilstein test?
answer
tests for the presence of halogens copper wire flame test should glow green/blue for Br
question
What is the jones test?
answer
test for the presence of secondary alcohols (regiochemistry)
question
For the jones test what does the orange/red color indicate?
answer
(-) the OH is tertiary
question
for the jones test what does the green color indicate?
answer
(+) the OH is secondary
question
In this we reaction, what are the states of our reactants and products?
answer
liquid reactant --> liquid product
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