
Concept explainers
(a)
Interpretation:
The major product obtained on treating the compounds in problem 29 with
Concept introduction:
Radical or free radical: unpaired valence electron of an atom, molecule, or ion is called as radical.
Bond strength is depends on the formation of the radical, if the radical is involving in resonance which is weakest bond strength.
Bromination:
1-Methyl cyclohexane is undergoes radical bromination which forms 1-bromo-1-methyl cyclohexane therefore, bromination will occur where the tertiary radical is present. Because bromination will occur selectively in tertiary alkyl radical. (bromination reactions are more selective reaction)
(b)
Interpretation:
The major product obtained on treating the compounds in problem 29 with
Concept introduction:
Radical or free radical: unpaired valence electron of an atom, molecule, or ion is called as radical.
Bond strength is depends on the formation of the radical, if the radical is involving in resonance which is weakest bond strength.
Bromination:
1-Methylcyclohexane is undergoes radical bromination which forms 1-bromo-1-methylcyclohexane therefore, bromination will occur where the tertiary radical is present. Because bromination will occur selectively in tertiary alkyl radical. (bromination reactions are more selective reaction)
(c)
Interpretation:
The major product obtained on treating the compounds in problem 29 with
Concept introduction:
Radical or free radical: unpaired valence electron of an atom, molecule, or ion is called as radical.
Bond strength is depends on the formation of the radical, if the radical is involving in resonance which is weakest bond strength.
Bromination:
1-Methylcyclohexane is undergoes radical bromination which forms 1-bromo-1-methylcyclohexane therefore, bromination will occur where the tertiary radical is present. Because bromination will occur selectively in tertiary alkyl radical. (bromination reactions are more selective reaction)

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Chapter 12 Solutions
Organic Chemistry, Books a la Carte Edition (8th Edition)
- Please help me solve this reaction.arrow_forwardIndicate the products obtained by mixing 2,2-dimethylpropanal with acetaldehyde and sodium ethoxide in ethanol.arrow_forwardSynthesize 2-Ethyl-3-methyloxirane from dimethyl(propyl)sulfonium iodide using the necessary organic or inorganic reagents. Draw the structures of the compounds.arrow_forward
- Synthesize 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_forwardSynthesize N-Methylcyclohexylamine from cyclohexanol using the necessary organic or inorganic reagents. Draw the structures of the compounds.arrow_forward
- 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
