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- https://chem.libretexts.org/Courses/Williams_School/Chemistry_II/04%3A_Organic_Functional_Groups/4.11%3A_Carboxylic_AcidsCarboxylic acids are important natural products and synthetic precursors. The common names are provided for carboxylic acids (1 to 10 carbons) and selected dicarboxylic acids.
- https://chem.libretexts.org/Bookshelves/Organic_Chemistry/Basic_Principles_of_Organic_Chemistry_(Roberts_and_Caserio)/18%3A_Carboxylic_Acids_and_Their_Derivatives/18.01%3A_Prelude_to_Carboxylic_Acids_and_Their_DerivativesAlmost all of the basic types of reactions now have been covered: addition, elimination, substitution, and rearrangement by polar, radical, and concerted mechanisms. Indeed, if you have been looking f...Almost all of the basic types of reactions now have been covered: addition, elimination, substitution, and rearrangement by polar, radical, and concerted mechanisms. Indeed, if you have been looking for similarities, you will have seen that most of the reactions discussed in the preceding three chapters are variations on basic types we have discussed earlier.
- https://chem.libretexts.org/Courses/Fullerton_College/Beginning_Chemistry_(Chan)/17%3A_Organic_Chemistry/17.05%3A_Other_Oxygen-Containing_Functional_GroupsAldehydes, ketones, carboxylic acids, esters, and ethers have oxygen-containing functional groups.
- https://chem.libretexts.org/Courses/Bellingham_Technical_College/CHEM_110%3A_Bellingham_Technical_College/03%3A_Module_3/3.05%3A_Other_Oxygen-Containing_Functional_GroupsAldehydes, ketones, carboxylic acids, esters, and ethers have oxygen-containing functional groups.
- https://chem.libretexts.org/Courses/can/CHEM_232_-_Organic_Chemistry_II_(Puenzo)/06%3A_Carboxylic_Acids_and_Nitriles/6.02%3A_Naming_Carboxylic_Acids_and_NitrilesSalts of carboxylic acids are named by writing the name of the cation followed by the name of the carboxylic acid with the –ic acid ending replaced by an –ate ending. It is not necessary to include th...Salts of carboxylic acids are named by writing the name of the cation followed by the name of the carboxylic acid with the –ic acid ending replaced by an –ate ending. It is not necessary to include the location number in the name because it is assumed that the functional group will be on the end of the parent chain.
- https://chem.libretexts.org/Courses/Martin_Luther_College/Organic_Chemistry_-_MLC/04%3A_Carbonyls/4.02%3A_Carboxylic_Acids/4.2.02%3A_Naming_Carboxylic_Acids_and_NitrilesSalts of carboxylic acids are named by writing the name of the cation followed by the name of the acid with the –ic acid ending replaced by an –ate ending. Open chain nitriles are named with the word ...Salts of carboxylic acids are named by writing the name of the cation followed by the name of the acid with the –ic acid ending replaced by an –ate ending. Open chain nitriles are named with the word -nitrile after the name of the parent alkane name (include the carbon atom of the nitrile as part of the parent - as in the example CH 3 CN has two carbons including the nitrile carbon, therefore it is ethanenitrile).
- https://chem.libretexts.org/Courses/Smith_College/Organic_Chemistry_(LibreTexts)/20%3A_Carboxylic_Acids_and_Nitriles/20.02%3A_Naming_Carboxylic_Acids_and_NitrilesSalts of carboxylic acids are named by writing the name of the cation followed by the name of the acid with the –ic acid ending replaced by an –ate ending. Open chain nitriles are named with the word ...Salts of carboxylic acids are named by writing the name of the cation followed by the name of the acid with the –ic acid ending replaced by an –ate ending. Open chain nitriles are named with the word -nitrile after the name of the parent alkane name (include the carbon atom of the nitrile as part of the parent - as in the example CH 3 CN has two carbons including the nitrile carbon, therefore it is ethanenitrile).
- https://chem.libretexts.org/Bookshelves/Organic_Chemistry/Organic_Chemistry_(Morsch_et_al.)/20%3A_Carboxylic_Acids_and_Nitriles/20.01%3A_Naming_Carboxylic_Acids_and_NitrilesThis section focuses on the IUPAC naming of carboxylic acids and nitriles, detailing how to write and interpret their names and structures. It emphasizes understanding the priority of functional group...This section focuses on the IUPAC naming of carboxylic acids and nitriles, detailing how to write and interpret their names and structures. It emphasizes understanding the priority of functional groups, especially for molecules with multiple functionalities, and highlights key naming conventions. Common and IUPAC names for carboxylic acids and the process for naming salts, dicarboxylic acids, and nitriles are explained.
- https://chem.libretexts.org/Bookshelves/Organic_Chemistry/Organic_Chemistry_II_(Morsch_et_al.)/20%3A_Carboxylic_Acids_and_Nitriles/20.01%3A_Naming_Carboxylic_Acids_and_NitrilesSalts of carboxylic acids are named by writing the name of the cation followed by the name of the carboxylic acid with the –ic acid ending replaced by an –ate ending. It is not necessary to include th...Salts of carboxylic acids are named by writing the name of the cation followed by the name of the carboxylic acid with the –ic acid ending replaced by an –ate ending. It is not necessary to include the location number in the name because it is assumed that the functional group will be on the end of the parent chain.
- https://chem.libretexts.org/Courses/University_of_Kansas/General%2C_Organic%2C_and_Biological_Chemistry/11%3A_Organic_Chemistry/11.04%3A_Other_Oxygen-Containing_Functional_GroupsAldehydes, ketones, carboxylic acids, esters, and ethers have oxygen-containing functional groups.
- https://chem.libretexts.org/Courses/Smith_College/CHM_222_Chemistry_II%3A_Organic_Chemistry_(2025)/11%3A_Carboxylic_Acids_and_Nitriles/11.02%3A_Naming_Carboxylic_Acids_and_NitrilesSalts of carboxylic acids are named by writing the name of the cation followed by the name of the carboxylic acid with the –ic acid ending replaced by an –ate ending. It is not necessary to include th...Salts of carboxylic acids are named by writing the name of the cation followed by the name of the carboxylic acid with the –ic acid ending replaced by an –ate ending. It is not necessary to include the location number in the name because it is assumed that the functional group will be on the end of the parent chain.
