
(a)
Interpretation:
The structure of the product obtained by the reaction between propene and hydrogen gas in the presence of metal catalyst should be determined.
Concept introduction:
The addition on the alkene is the electrophilic addition reaction. In this reaction, electrophile reacts with carbon-carbon double of the alkene which results in the formation of
The hydrogenation of
A nucleophile is the Lewis base that donates an electron pair to form a covalent bond with the electrophile.
An electrophile is the Lewis acid that accepts the electron to form a bond with the nucleophile.
(b)
Interpretation:
The structure of the product obtained upon heating
Concept introduction:
The preparation of alkene is the type of elimination reaction.
The
The
A nucleophile is the Lewis base that donates an electron pair to form a covalent bond with the electrophile. An electrophile is the Lewis acid that accepts the electron to form a bond with the nucleophile.
The good leaving groups are the weak base. They can be an anion or neutral molecule.

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Chapter 27 Solutions
General Chemistry: Principles and Modern Applications (11th Edition)
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- If possible, please provide the formula of the compound 3,3-dimethylbut-2-enal.arrow_forwardSynthesize 1,4-dibromobenzene from acetanilide (N-phenylacetamide) using the necessary organic or inorganic reagents. Draw the structures of the compounds.arrow_forwardIndicate the products obtained by mixing (3-oxo-3-phenylpropyl)triphenylphosphonium bromide with sodium hydride.arrow_forward
- We 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_forwardIndicate the products obtained by mixing 2-Propanone and ethyllithium and performing a subsequent acid hydrolysis.arrow_forward
- Indicate 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_forwardIndicate the products obtained if 2,2-dimethylpropanal and acetaldehyde are mixed with sodium ethoxide in ethanol.arrow_forward
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