Concept explainers
a)
Interpretation:
The IUPAC name of the
Concept introduction:
The longest continuous carbon chain in the molecule is chosen. The chain is numbered from the end which gives lowest number to the substituent either halo or alkyl group present. If different halogens are present they are numbered and listed in the alphabetical order while writing the name. If same two alternatives exist for different substituents, then the chain is numbered from the end that gives lowest number to the substituent that has alphabetical preference.
To give:
The IUPAC name of the alkyl halide shown.
b)
Interpretation:
The IUPAC name of the alkyl halide is to be given.
Concept introduction:
The longest continuous carbon chain in the molecule is chosen. The chain is numbered from the end which gives lowest number to the substituent either halo or alkyl group present. If different halogens are present they are numbered and listed in the alphabetical order while writing the name. If same two alternatives exist for different substituents, then the chain is numbered from the end that gives lowest number to the substituent that has alphabetical preference.
To give:
The IUPAC name of the alkyl halide shown.
c)
Interpretation:
The IUPAC name of the alkyl halide is to be given.
Concept introduction:
The longest continuous carbon chain in the molecule is chosen. The chain is numbered from the end which gives lowest number to the substituent either halo or alkyl group present. If different halogens are present they are numbered and listed in the alphabetical order while writing the name. If same two alternatives exist for different substituents, then the chain is numbered from the end that gives lowest number to the substituent that has alphabetical preference.
To give:
The IUPAC name of the alkyl halide shown.
d)
Interpretation:
The IUPAC name of the alkyl halide is to be given.
Concept introduction:
The longest continuous carbon chain in the molecule is chosen. The chain is numbered from the end which gives lowest number to the substituent either halo or alkyl group present. If different halogens are present they are numbered and listed in the alphabetical order while writing the name. If same two alternatives exist for different substituents, then the chain is numbered from the end that gives lowest number to the substituent that has alphabetical preference.
To give:
The IUPAC name of the alkyl halide shown.
e)
Interpretation:
The IUPAC name of the alkyl halide is to be given.
Concept introduction:
The longest continuous carbon chain in the molecule is chosen. The chain is numbered from the end which gives lowest number to the substituent either halo or alkyl group present. If different halogens are present they are numbered and listed in the alphabetical order while writing the name. If same two alternatives exist for different substituents, then the chain is numbered from the end that gives lowest number to the substituent that has alphabetical preference.
To give:
The IUPAC name of the alkyl halide shown.
f)
Interpretation:
The IUPAC name of the alkyl halide is to be given.
Concept introduction:
The longest continuous carbon chain in the molecule is chosen. The chain is numbered from the end which gives lowest number to the substituent either halo or alkyl group present. If different halogens are present they are numbered and listed in the alphabetical order while writing the name. If same two alternatives exist for different substituents, then the chain is numbered from the end that gives lowest number to the substituent that has alphabetical preference.
To give:
The IUPAC name of the alkyl halide shown.
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Chapter 10 Solutions
ORGANIC CHEMISTRY-EBOOK>I<
- Give the IUPAC name of this structure. Br COOH NO₂arrow_forwardGive the common name for NN OH T CH3-CH₂-C-N-CH₂-CH3 Spell out the common name of the compound. Give the IUPAC name for 0 CH₂ || CH₂-C-N-CH₂-CH₂-CH₂, Spell out the IUPAC name of the compound. diethylamine Draw all missing reactants and/or products in the appropriate boxes by placing atoms on the canvas and connecting them with bonds. Add charges where needed. HE CONT HOarrow_forwardDraw the structure of (R) 3-hydroxy-4-cyclohexenone. Give the IUPAC name of this compound, including stereochemistry. CH₂ HỌ.Harrow_forward
- Why can formaldehyde (CH20) be prepared in the form of a 37% solution in water, whereas octanal cannot? (Select all that apply.) | Octanal is more hydrophilic than formaldehyde. O Formaldehyde is a small molecule. O Formaldehyde is polar. O Octanal is mostly hydrophobic.arrow_forwardAlkyl sulfonates undergo the same type of substitution reactions as alkyl halides and can also be prepared from alcohols. What advantage does the preparation of an alkyl sulfonate from an alcohol have over the preparation of an alkyl halide from an alcohol?arrow_forwardGive the IUPAC name for the alkyl halide below.arrow_forward