(a)
Interpretation: The arrow pushing method is to be interpreted for the given transformation.
Concept introduction: The chemical transformation can occur with the hydride shift; methylene shifts or methyl shifts etc.
Each transformation can be shown by the arrow pushing method in which the curved arrows show the movement of electrons or protons. The chemical transformation leads to the formation of intermediates.
(b)
Interpretation: The arrow pushing method is to be interpreted for the given transformation.
Concept introduction: The chemical transformation can occur with the hydride shift; methylene shifts or methyl shifts etc.
Each transformation can be shown by the arrow pushing method in which the curved arrows show the movement of electrons or protons. The chemical transformation leads to the formation of intermediates.
(c)
Interpretation: The arrow pushing method is to be interpreted for the given transformation.
Concept introduction: The chemical transformation can occur with the hydride shift; methylene shifts or methyl shifts etc.
Each transformation can be shown by the arrow pushing method in which the curved arrows show the movement of electrons or protons. The chemical transformation leads to the formation of intermediates.
(d)
Interpretation: The arrow pushing method is to be interpreted for the given transformation.
Concept introduction: The chemical transformation can occur with the hydride shift; methylene shifts or methyl shifts etc.
Each transformation can be shown by the arrow pushing method in which the curved arrows show the movement of electrons or protons. The chemical transformation leads to the formation of intermediates.

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Chapter 6 Solutions
ORGANIC CHEMISTRY (LL)-W/WILEYPLUS
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- Indicate the products obtained by mixing (3-oxo-3-phenylpropyl)triphenylphosphonium bromide with sodium hydride.arrow_forwardWe mix N-ethyl-2-hexanamine with excess methyl iodide and followed by heating with aqueous Ag2O. Indicate the major products obtained.arrow_forwardIndicate the products obtained by mixing acetophenone with iodine and NaOH.arrow_forward
- Indicate the products obtained by mixing 2-Propanone and ethyllithium and performing a subsequent acid hydrolysis.arrow_forwardIndicate the products obtained if (E)-2-butenal and 3-oxo-butanenitrile are mixed with sodium ethoxide in ethanol.arrow_forwardQuestion 3 (4 points), Draw a full arrow-pushing mechanism for the following reaction Please draw all structures clearly. Note that this intramolecular cyclization is analogous to the mechanism for halohydrin formation. COH Br + HBr Brarrow_forward
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