Homework Answers
1. First 3 step are known as
enamine synthesise, in which amine and ketone will form
enamine.
2. Then lonepair of nitrogen involve and enamine will attack on aldehyde followed by dehydration.
3. Finally ring will go aromatisation to get our desired product.
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Synthesis of 1-Bromobutane: An SN2 Reaction Pre-Laboratory Exercises PRE-LABORATORY EXERCISES NAME: Cynthesis of 1-Bromobutane: An SN...
Synthesis of 1-Bromobutane: An SN2 Reaction Pre-Laboratory
Exercises
PRE-LABORATORY EXERCISES NAME: Cynthesis of 1-Bromobutane: An SN 2 Reaction Butylbromide was prepared by refluxing in a 100-ml round bottomed flask a solution containing 13:35 Br 15 ml of water, 10 mL of n-butyl alcohol. 15 ml of concentrated H.SO. and a few boiling stories, 1. 2. R." d 1.275 laborales Nel CH3CH2CH2CH2OH + NaBr H2SO4 Superletalyst CHCH2CH2CHBr + NaHSO + HO (eq. 16) 1-butanol bp 118 C 1-bromobutane d 0.810 bp...
Need help, numbers 3-6 please show work. and fill out table of chemicals for all chemical...
Need help, numbers 3-6 please show work. and fill out table of
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calculate mmol in the table as well show work please
and each of these must be listed in its own row. There are 10 column headings: IUPAC name OR common name, structure, CAS number (Chemical Abstract Service number) molecular mass, melting point (if applicable), boiling point (if applicable), solubility (in water, if applicable), density, amounts to be used in the experiment, and the...
Please help!!! The Chemistry of Cocaine by Brahmadeo Dewprashad Department of Science Borough of Manhattan Community...
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The following questions are from an experiment titled Friedel-Crafts Alkylation for Organic Chemistry II Lab. There...
The following questions are from an experiment titled
Friedel-Crafts Alkylation for Organic Chemistry II Lab. There are
pictures attached of the lab manual.
2) Is this method a good route for the preparation of
p-sec-butyltoulene? Give reasons for your answer.
3) Why do you use a large excess of toulene. What are its
functions?
4) What is the purpose for adding the hydrochloric acid to the
water in the separatory funnel in step 5? Hint: If no acid is
added,...
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The scheme below shows the synthesis of an antihypertensitive agent (drug used to treat high blood pressure). Answer the questions that follows. a Br 1 Br CI с CO Me + Meo H2NCO Me (Question 3) B OME CN CN CN CN 6 2 3 4 5 CO Me CO Me Buz SnNz d Final product (9) (1) KOH, heat (2) H+ work up partial hydrolysis (Question 4) CAH, CAH, CN 7 NH NEN 8 Question 1 Select the best...
Synthesis of 1-Bromobutane: An SN2 Reaction Pre-Laboratory
Exercises
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Need help, numbers 3-6 please show work. and fill out table of
chemicals for all chemical used.
calculate mmol in the table as well show work please
and each of these must be listed in its own row. There are 10 column headings: IUPAC name OR common name, structure, CAS number (Chemical Abstract Service number) molecular mass, melting point (if applicable), boiling point (if applicable), solubility (in water, if applicable), density, amounts to be used in the experiment, and the...
Please help!!!
The Chemistry of Cocaine by Brahmadeo Dewprashad Department of Science Borough of Manhattan Community College, The City University of New York Professor Martinez entered the classroom with a livelier step than usual. Her morning students were accustomed to their instructor's ritual of carefully unpacking her book bag and arranging the contents neatly on the desk before beginning a lecture. But this time Martinez simply set her bag down on the chair, turned to the class, and began. "Today,...
The following questions are from an experiment titled
Friedel-Crafts Alkylation for Organic Chemistry II Lab. There are
pictures attached of the lab manual.
2) Is this method a good route for the preparation of
p-sec-butyltoulene? Give reasons for your answer.
3) Why do you use a large excess of toulene. What are its
functions?
4) What is the purpose for adding the hydrochloric acid to the
water in the separatory funnel in step 5? Hint: If no acid is
added,...
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