
Concept explainers
(a)
Interpretation:
The IUPAC name for the given structure of acid chloride is to be provided.
Concept introduction:
The IUPAC name of a compound is written from its structure. The IUPAC name is made up of three parts: prefix, root, and suffix. The suffix indicates the highest-priority functional group present. Its location is written as a prefix, unless redundant. The root is the longest continuous carbon chain that also includes the highest priority functional group. The carbon atom of the highest functional group must be the part of the longest continuous chain of carbon atoms, and the numbering starts from that carbon. Any other
For acid chlorides, the highest priority functional group is the
If any chiral carbons are present, their absolute configurations are specified at the start along with the carbon number if necessary. A di, tri, etc., before a prefix or suffix indicates the number of instances of that functional group.
(b)
Interpretation:
The IUPAC name for the given structure of acid chloride is to be provided.
Concept introduction:
The IUPAC name of a compound is written from its structure. The IUPAC name is made up of three parts: prefix, root, and suffix. The suffix indicates the highest-priority functional group present. Its location is written as a prefix, unless redundant. The root is the longest continuous carbon chain that also includes the highest priority functional group. The carbon atom of the highest functional group must be the part of the longest continuous chain of carbon atoms, and the numbering starts from that carbon. Any other functional groups present are listed alphabetically as prefixes along with their locant numbers.
For acid chlorides, the highest priority functional group is the carboxylic acid chloride group (
(c)
Interpretation:
The IUPAC name for the given structure of acid chloride is to be provided.
Concept introduction:
The IUPAC name of a compound is written from its structure. The IUPAC name is made up of three parts: prefix, root, and suffix. The suffix indicates the highest-priority functional group present. Its location is written as a prefix, unless redundant. The root is the longest continuous carbon chain that also includes the highest priority functional group. The carbon atom of the highest functional group must be the part of the longest continuous chain of carbon atoms, and the numbering starts from that carbon. Any other functional groups present are listed alphabetically as prefixes along with their locant numbers.
For acid chlorides, the highest priority functional group is the carboxylic acid chloride group (

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Chapter F Solutions
Organic Chemistry: Principles And Mechanisms
- Determine the pH of solution of HC3H5O2 By constructing an ICE table writing the equilibrium constant expression, and using this information to determine the pH. The Ka of HC3H5O2 is 1.3 x 10-5arrow_forwardDetermine if the following salt is neutral, acidic or basic. If acidic or basic, write the appropriate equilibrium equation for the acid or base that exists when the salt is dissolved in aqueous solution. If neutral, simply write only NR. Be sure to include the proper phases for all species within the reaction LiNO3arrow_forwardAn unknown weak acid with a concentration of 0.410 M has a pH of 5.600. What is the Ka of the weak acid?arrow_forward
- (racemic) 19.84 Using your reaction roadmaps as a guide, show how to convert 2-oxepanone and ethanol into 1-cyclopentenecarbaldehyde. You must use 2-oxepanone as the source of all carbon atoms in the target molecule. Show all reagents and all molecules synthesized along the way. & + EtOH H 2-Oxepanone 1-Cyclopentenecarbaldehydearrow_forwardR₂ R₁ R₁ a R Rg Nu R₂ Rg R₁ R R₁₂ R3 R R Nu enolate forming R₁ R B-Alkylated carbonyl species or amines Cyclic B-Ketoester R₁₁ HOB R R₁B R R₁₂ B-Hydroxy carbonyl R diester R2 R3 R₁ RB OR R₂ 0 aB-Unsaturated carbonyl NaOR Aldol HOR reaction 1) LDA 2) R-X 3) H₂O/H₂O ketone, aldehyde 1) 2°-amine 2) acid chloride 3) H₂O'/H₂O 0 O R₁ R₁ R R₁ R₁₂ Alkylated a-carbon R₁ H.C R₁ H.C Alkylated methyl ketone acetoacetic ester B-Ketoester ester R₁ HO R₂ R B-Dicarbonyl HO Alkylated carboxylic acid malonic ester Write the reagents required to bring about each reaction next to the arrows shown. Next, record any regiochemistry or stereochemistry considerations relevant to the reaction. You should also record any key aspects of the mechanism, such as forma- tion of an important intermediate, as a helpful reminder. You may want to keep track of all reactions that make carbon-carbon bonds, because these help you build large molecules from smaller fragments. This especially applies to the reactions in…arrow_forwardProvide the reasonable steps to achieve the following synthesis.arrow_forward
