If 1-pentanol, butanoic acid, and a catalytic amount of H2SO4 were refluxed in toluene with the same set up and conditions as experiment 8, the organic product(s) of the reaction would be? Butyl pentanoate. Pentyl butanoate. Pentyl butyl ether. Both butyl pentanoate and pentyl butanoate. No reaction would occur.

If 1-pentanol, butanoic acid, and a catalytic amount of H2SO4 were refluxed in toluene with the same set up and conditions as experiment 8, the organic product(s) of the reaction would be? Butyl pentanoate. Pentyl butanoate. Pentyl butyl ether. Both butyl pentanoate and pentyl butanoate. No reaction would occur.

Macroscale and Microscale Organic Experiments

7th Edition

ISBN:9781305577190

Author:Kenneth L. Williamson, Katherine M. Masters

Publisher:Kenneth L. Williamson, Katherine M. Masters

Chapter18: Radical Initiated Chlorination Of 1-chlorobutane

Section: Chapter Questions

Problem 1Q

See similar textbooks

Similar questions

What is the strongest IMF in pure 2-octanone? I know it is a ketone and has some polarity due to this, but the carbon chain so long, I wonder if london dispersion forces are stronger?
Ethanol, isopropyl alcohol, and n-propyl alcohol may all be used as ingredients in hand sanitizer. Which of those three could be made most easily by reduction of acetone (CHCOCH3) with a hydride reagent?
In the lab for the synthesis of methyl m-nitrobenzoate from methyl benzoate using HNO3 and H2SO4 via EAS, the product is recrystallized to remove impurities using 95% ethanol. Would o-nitrobenzoate and methyl p-nitrobenzoate be considered impurities? If that is so, how come ethanol can remove o-nitrobenzoate and methyl p-nitrobenzoate, but has no effect on m-nitrobenzoate? Thank you.
Oxidation of a primary alcohol with pyridinium chlorochromate ( PCC, C5H6NCrO3Cl) would yield what?
In which of the statements given below, the event is not an oxidation reaction? A. Product formation as a result of the reaction of benzoine with nitric acid B. Formation of the product as a result of the reaction of 2-propene at KMnO4 / Basic ambient temperature C. Formation of the product as a result of the reaction of 2-propene in KMnO4 / Basic medium cold D. CH3CH2OH + KMnO4 → CH3COOH E. Reaction of an alkyl halide with ammonia
NH4Cl is sometimes preferred instead of HCl or H2SO4 for “acid” work-up after Grignard reactions, particularly when the expected and desired product is a tertiary alcohol: why?
1. Esters can be synthesized from the nucleophilic substitution reaction of anhydrides and alcohol in the presence of a base give a complete mechanism and the final product for the reaction below 2. using appropriate illustrations, explain what is meant by the tetrahedral transition state( also indicate the geometry for the starting material and product).
Phineas and Ferbs, two brothers who enjoy vacations, doing fun things every summer. This summer the brothers and their friends carry out an organic synthesis with an unknown compound (L1) that contains 52% Carbon, 6% Hydrogen and 42% bromine, this compound (L1) is treated with magnesium in ether to obtain L2 , which reacts violently with D2O for 1-methyl cyclohexene with a deuterium atom in the methyl group (L3). The L2 reaction is treated with acetone followed by hydrolysis to give L4. Heating L4 with concentrated sulfuric acid gives L5, which decolors the bromine, obtaining L6. L5 undergoes hydrogenation with excess hydrogen and platinum as a catalyst giving rise to isobutyl cyclohexane. Determine the structures of compounds L1 through L6.
How many mono-chlorination products are possible for 3-methylpentane? Draw them out.
Alkene can be prepared from alcohol using acid catalyzed dehydration reaction a. Draw and label the main aparatus and general important reagents that involved in the distillation process for this reaction. b. Suggest three (3) laboratory safety rules while conducting the reaction in 2(a) c. The prepared alkene reacts with bromine water with the presence of concentrated sulphuric acid. Suggest the reaction and explain your answer.
Starting with 1-butanol, provide a synthetic scheme to make 4-methyl-4 hexanol, including intermediate products.
Name, draw and describe the organic product of the reaction between 2-methylbut-1-ene and H2O in the presence of H2SO4 and provide a clear rationale as to why this is the major product of the reaction and the minor product of the reaction.