
a) Ethyl 1-ethylpropyl ether
Interpretation:
The structure of ethyl 1-ethylpropyl ether is to be drawn.
Concept introduction:
Simple ethers are with no other
To draw:
The structure of ethyl 1-ethylpropyl ether.
b) Di (p-chlorophenyl) ether
Interpretation:
The structure of di (p-chlorophenyl) ether is to be drawn.
Concept introduction:
Simple ethers are with no other functional groups are named by identifying the two organic substituents and adding the word ether. If other functional groups are present, the ether part is considered as an alkoxy substituent.
To give:
The structure of di(p-chlorophenyl) ether.
c) 3, 4-Dimethoxybenzoic acid
Interpretation:
The structure of 3, 4-dimethoxybenzoic acid ether is to be drawn.
Concept introduction:
Simple ethers are with no other functional groups are named by identifying the two organic substituents and adding the word ether. If other functional groups are present, the ether part is considered as an alkoxy substituent.
To give:
The structure of 3, 4-dimethoxybenzoic acid.
d) Cyclopentyloxycyclohexane
Interpretation:
The structure of cyclopentyloxycyclohexane is to be drawn.
Concept introduction:
Simple ethers are with no other functional groups are named by identifying the two organic substituents and adding the word ether. If other functional groups are present, the ether part is considered as an alkoxy substituent.
To give:
The structure of cyclopentyloxycyclohexane.
e) 4-Allyl-2-methoxyphenol (eugenol)
Interpretation:
The structure of 4-allyl-2-methoxyphenol (eugenol) is to be drawn.
Concept introduction:
Simple ethers are with no other functional groups are named by identifying the two organic substituents and adding the word ether. If other functional groups are present, the ether part is considered as an alkoxy substituent.
To give:
The structure of 4-allyl-2-methoxyphenol (eugenol).

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Chapter 18 Solutions
Study Guide with Student Solutions Manual for McMurry's Organic Chemistry, 9th
- 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
- Synthesize N-Methylcyclohexylamine from cyclohexanol using the necessary organic or inorganic reagents. Draw the structures of the compounds.arrow_forwardIf 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_forward
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- 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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