(a)
Interpretation:
Among the given formulas, the one which cannot be the correct formula for the organic compounds is to be predicted.
Concept introduction:
Degree of unsaturation or unsaturation number is used to determine the total number of rings and pi bonds present in compound by just looking at the molecular formula. It does not specify the total number of rings and total number of pi bonds individually.
(b)
Interpretation:
The constitutional isomers of the compounds with the formula
Concept introduction:
Degree of unsaturation or unsaturation number is used to determine the total number of rings and pi bonds present in compound by just looking at the molecular formula. It does not specify the total number of rings and total number of pi bonds individually.

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Chapter 4 Solutions
EBK ORGANIC CHEMISTRY STUDY GUIDE AND S
- Synthesize 2-Ethyl-3-methyloxirane from dimethyl(propyl)sulfonium iodide using the necessary organic or inorganic reagents. Draw the structures of the compounds.arrow_forwardSynthesize 2-Hydroxy-2-phenylacetonitrile from phenylmethanol using the necessary organic or inorganic reagents. Draw the structures of the compounds.arrow_forwardSynthesize N-Methylcyclohexylamine from cyclohexanol using the necessary organic or inorganic reagents. Draw the structures of the compounds.arrow_forward
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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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