Click the "draw structure" button to launch the drawing utility.Under certain reaction conditions, 2,3-dibromobutane reacts with two equivalents of base to give threeproducts, each of which contains two new T bonds. Product A has two sp hybridized carbon atoms,product B has one sp hybridized carbon atom, and product C has none. What is the structure of C?

The given information shows that the 2,3 dibromoethane reacts with 2 equivalents of a base to give 3…

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Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter14: Conjugated Compounds And Ultraviolet Spectroscopy

Section14.SE: Something Extra

Problem 65AP: The double bond of an enamine (alkene + amine) is much more nucleophilic than a typical alkene...

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Under certain reaction conditions, 2,3-dibromobutane reacts with twoequivalents of base to give three products, each of which contains twonew π bonds. Product A has two sp hybridized carbon atoms, product Bhas one sp hybridized carbon atom, and product C has none. What arethe structures of A, B, and C?
Define the below statement ? Benzene's six π electrons make it electron rich, so it reacts withelectrophiles.
Compound A exhibits a peak in its 1H NMR spectrum at 7.6 ppm, indicating that it is aromatic. (a) How are the carbon atoms of the triple bonds hybridized? (b) In what type of orbitals are the π electrons of the triple bonds contained? (c) How many π electrons are delocalized around the ring in A?
Rank the compounds in each set in order of increasing acid strength.(a) CH3CH2COOH CH3CHBrCOOH CH3CBr2COOH
Predict which member of each pair has the higher boiling point, and explain the reasons for your predictions.(a) hexan-1-ol or 3,3-dimethylbutan-1-ol (b) hexan-2-one or hexan-2-ol
Compound A has molecular formula C7H15B.. Treatment of compound A with sodium ethoxide yields only one elimination product (compound B) and no substitution products. When compound B is treated with dilute sulfuric acid, compound C is obtained, which has molecular formula C7H160. Draw the structures of compounds A, B, and C.
Consider the tetracyclic aromatic compound drawn below, with rings labeled as A, B, C, and D. (a) Which of the four rings is most reactive in electrophilic aromatic substitution? (b) Which of the four rings is least reactive in electrophilic aromatic substitution? (c) What are the major product(s) formed when this compound is treated with one equivalent of Br2?
There are three compounds with same molecular formula C8H9Br, andit has been known that all these three compounds contain a phenyl ring, anethyl group, and a bromide atom. A cannot react with AgNO3. B reactswith AgNO3 smoothly at room temperature. C can react with AgNO3 athigh temperature. Try to give the structures of A, B and C.
Explain why pentane-2,4-dione forms two alkylation products (A and B) when the number ofequivalents of base is increased from one to two.
Write out the two-step sequence that converts benzene to each compound.
(a) Draw all products formed by treatment of each dibromide (A and B) with one equivalent of NaNH2. (b) Label pairs of diastereomers and constitutional isomers. H Br H Br CH3 CH3 Br H H Br A
When trans-2-chloro-1-cyclohexanol is treated with a base, cyclohexene oxide is the product. However, when cis-2-chloro-1-cyclohexanol is treated with a base, the product is cyclohexanone. Why doesn’t the cis isomer yield the oxide?

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