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- https://chem.libretexts.org/Courses/Honolulu_Community_College/CHEM_100%3A_Chemistry_and_Society/10%3A_Organic_Chemistry/10.03%3A_Branched_HydrocarbonsA unique name can be given to branched hydrocarbons. A unique structure can be drawn for the name of a hydrocarbon.
- https://chem.libretexts.org/Courses/University_of_Kansas/General%2C_Organic%2C_and_Biological_Chemistry/11%3A_Organic_Chemistry/11.02%3A_Branched_HydrocarbonsA unique name can be given to branched hydrocarbons. A unique structure can be drawn for the name of a hydrocarbon.
- https://chem.libretexts.org/Courses/University_of_Kansas/CHEM_110%3A_Introductory_Chemistry_(Sharpe_Elles)_SP25/11%3A_Organic_Chemistry/11.02%3A_Branched_HydrocarbonsA unique name can be given to branched hydrocarbons. A unique structure can be drawn for the name of a hydrocarbon.
- https://chem.libretexts.org/Courses/Georgia_Southern_University/CHEM_1152%3A_Survey_of_Chemistry_II_(Osborne)/04%3A_Organic_Nomenclature_-_Carbonyl-Containing_Compounds/4.05%3A_EstersAn ester has an OR group attached to the carbon atom of a carbonyl group.
- https://chem.libretexts.org/Bookshelves/Organic_Chemistry/Basic_Principles_of_Organic_Chemistry_(Roberts_and_Caserio)/03%3A_Organic_Nomenclature/3.02%3A_AlkanesThe most definitive set of organic nomenclature rules currently in use were evolved through several international conferences and are known as the International Union of Pure and Applied Chemistry Rul...The most definitive set of organic nomenclature rules currently in use were evolved through several international conferences and are known as the International Union of Pure and Applied Chemistry Rules (IUPAC rules). We first shall describe this system for naming the hydrocarbons known as alkanes - the so-called saturated paraffin hydrocarbons that have no double or triple bonds, or rings.
- https://chem.libretexts.org/Bookshelves/Analytical_Chemistry/Analytical_Chemistry_2.1_(Harvey)/03%3A__The_Vocabulary_of_Analytical_Chemistry/3.09%3A_Additional_ResourcesThe page provides information about IUPAC's web-based compendium of analytical terminology and references to papers and texts discussing various schemes for classifying analytical methods. It lists wo...The page provides information about IUPAC's web-based compendium of analytical terminology and references to papers and texts discussing various schemes for classifying analytical methods. It lists works covering performance characteristics, debates on sensitivity, and analytical procedures for specific analytes, including notable textbooks and compilations. Additionally, it mentions a review of analytical methodology's significance in regulatory environments.
- https://chem.libretexts.org/Courses/Georgia_Southern_University/CHEM_1152%3A_Survey_of_Chemistry_II_(Osborne)/04%3A_Organic_Nomenclature_-_Carbonyl-Containing_Compounds/4.01%3A_Aldehydes_and_KetonesThe common names of aldehydes are taken from the names of the corresponding carboxylic acids: formaldehyde, acetaldehyde, and so on. The common names of ketones, like those of ethers, consist of the n...The common names of aldehydes are taken from the names of the corresponding carboxylic acids: formaldehyde, acetaldehyde, and so on. The common names of ketones, like those of ethers, consist of the names of the groups attached to the carbonyl group, followed by the word ketone. Stem names of aldehydes and ketones are derived from those of the parent alkanes, using an -al ending for an aldehydes and an -one ending for a ketone.
- https://chem.libretexts.org/Courses/Georgia_Southern_University/CHEM_1152%3A_Survey_of_Chemistry_II_(Osborne)/02%3A_Organic_Nomenclature_-_Unsaturated_Hydrocarbons/2.04%3A_Aromatic_CompoundsAromatic hydrocarbons appear to be unsaturated, but they have a special type of bonding and do not undergo addition reactions.
- https://chem.libretexts.org/Courses/Georgia_Southern_University/CHEM_1152%3A_Survey_of_Chemistry_II_(Osborne)/01%3A_CHEM_1151_Organic_Review/1.06%3A_CycloalkanesMany organic compounds have cyclic structures.
- https://chem.libretexts.org/Courses/Georgia_Southern_University/CHEM_1152%3A_Survey_of_Chemistry_II_(Osborne)/04%3A_Organic_Nomenclature_-_Carbonyl-Containing_Compounds/4.S%3A_Carbonyl-Containing_Compounds_(Summary)To ensure that you understand the material in this chapter, you should review the meanings of the following bold terms in the summary and ask yourself how they relate to the topics in the chapter.
- https://chem.libretexts.org/Courses/Lakehead_University/Analytical_I/4%3A_Evaluating_Analytical_Data/4.07%3A_Detection_LimitsA method’s detection limit as the smallest concentration or absolute amount of analyte that has a signal significantly larger than the signal from a suitable blank. Although our interest is in the amo...A method’s detection limit as the smallest concentration or absolute amount of analyte that has a signal significantly larger than the signal from a suitable blank. Although our interest is in the amount of analyte, in this section we will define the detection limit in terms of the analyte’s signal.
