Asked by Issac
Why was the tert butyl chloride washed with aqueous sodium hydrogen carbonate? what gas was evolved during the washing? Write a balance equation
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Answered by
Jonathan moses
Science
Answered by
Don Kapi
To neutralise the excess HCL.
Answered by
Patricia
Please need an answer on why was tert butyl chloride washed with aqueous sodium hydrogen carbonate? What gas was evolved during the washing and write a balanced equation .
Answered by
Patricia
Why was tert butyl chloride washed with aqueous sodium hydrogen carbonated?
Answered by
Thomas
Need an answer
Answered by
perilla
Why was thetert .Butyl chloride washed with aqueous sodium hydrogen carbonate ?What gas was evolved during the washing? Write a balanced equation.
Answered by
Alex
Need answers
Answered by
Donald J Kuk
answer for question
Answered by
frank
answers
Answered by
uta
to neutralise hcl
Answered by
Cecelia
Please I need the answer to the question that mentioned above.
Answered by
Danny
Why was the tert. Butyl chloride washed with aqueous sodium hydrogen carbonate? What gas was evolved during the washing? Write a balance equation.
Answered by
Danny
I want the answer to what is mentioned above about tert. Butyl chloride from
anyone willing to help.
anyone willing to help.
Answered by
KUMAWA
Yes
Answered by
Peter Lyangao Jr.
1. Why was the tert. Butyl chloride washed with aqueous sodium hydrogen carbonate? What
gas was evolved during the washing? Write a balance equation
2. Why was the tert.butyl chloride finally washed with water?
3. Write a balanced equation for the overall preparation. Since tert butanol was the limiting
reagent, calculate the theoretical yield (and % yield) of the tert.butyl chloride.
4. Given the following alcohol (i) 3-pentanol (ii) 2-pentanol (iii) 1-pentanol
(iv) 2-methyl-2-butanol:
(a) Draw the structures of the given alcohols and classify each as primary, secondary or
tertiary.
(b) Which of the given alcohols will react most rapidly with hydrogen bromide (HBr) and
which will react least rapidly? Write/draw the structure of the product in each case.
5. It is known that secondary and tertiary alcohols sometimes undergo rearrangement when
treated with hydrogen halides (HX) whilst primary alcohols do not. Mechanistically,
secondary and tertiary alcohols undergo reaction with HX by SN1 pathway while primary
alcohols by SN2 pathway.
With respect to the mechanism given, describe the importan
gas was evolved during the washing? Write a balance equation
2. Why was the tert.butyl chloride finally washed with water?
3. Write a balanced equation for the overall preparation. Since tert butanol was the limiting
reagent, calculate the theoretical yield (and % yield) of the tert.butyl chloride.
4. Given the following alcohol (i) 3-pentanol (ii) 2-pentanol (iii) 1-pentanol
(iv) 2-methyl-2-butanol:
(a) Draw the structures of the given alcohols and classify each as primary, secondary or
tertiary.
(b) Which of the given alcohols will react most rapidly with hydrogen bromide (HBr) and
which will react least rapidly? Write/draw the structure of the product in each case.
5. It is known that secondary and tertiary alcohols sometimes undergo rearrangement when
treated with hydrogen halides (HX) whilst primary alcohols do not. Mechanistically,
secondary and tertiary alcohols undergo reaction with HX by SN1 pathway while primary
alcohols by SN2 pathway.
With respect to the mechanism given, describe the importan
Answered by
Peter Lyangao Jr.
Please help solve any of the questions above
Answered by
Kaya
The solutions to the above mentioned questions.
Answered by
josh
to complete assignment
Answered by
SAMUEL
PLEASE KINDLY HELP MI WITH THE ANSWER
Answered by
chris
i need a answer please
Answered by
Relvie
Answers for the above questions please
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