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- https://chem.libretexts.org/Bookshelves/Organic_Chemistry/Organic_Chemistry_II_(Morsch_et_al.)/23%3A_Carbonyl_Condensation_Reactions/23.S%3A_Carbonyl_Condensation_Reactions_(Summary)To reverse the aldol reaction, break the C-C bond between the alpha carbon and the carbon attached to the hydroxy group. In 1,4 additions the nucleophile is added to the carbon β to the carbonyl while...To reverse the aldol reaction, break the C-C bond between the alpha carbon and the carbon attached to the hydroxy group. In 1,4 additions the nucleophile is added to the carbon β to the carbonyl while the hydrogen is added to the carbon α to the carbonyl. Skill 23.10 Identify the structural features necessary to ensure that two carbonyl compounds will react together in a mixed aldol reaction to give a single product rather than a mixture of products.
- https://chem.libretexts.org/Courses/can/CHEM_232_-_Organic_Chemistry_II_(Puenzo)/03%3A_Chemistry_of_Benzene_-_Reactions_of_Aromatic_Compounds/3.11%3A_Synthesis_of_Polysubstituted_BenzenesThe ability to plan a successful multi step synthesis of complex molecules is one of the goals of organic chemists. It requires a working knowledge of the uses and limitations of many organic reaction...The ability to plan a successful multi step synthesis of complex molecules is one of the goals of organic chemists. It requires a working knowledge of the uses and limitations of many organic reactions - not only which reactions to use, but when. A few examples follow:
- https://chem.libretexts.org/Courses/Smith_College/Organic_Chemistry_(LibreTexts)/07%3A_Alkenes-_Structure_and_Reactivity/7.05%3A_Naming_AlkenesAlkenes contain carbon-carbon double bonds and are unsaturated hydrocarbons with the molecular formula is CnH2n; this is also the same molecular formula as cycloalkanes. For straight chain alkenes, it...Alkenes contain carbon-carbon double bonds and are unsaturated hydrocarbons with the molecular formula is CnH2n; this is also the same molecular formula as cycloalkanes. For straight chain alkenes, it is the same basic rules as nomenclature of alkanes except change the suffix to "-ene."
- https://chem.libretexts.org/Courses/Remixer_University/A_Quick_Guide_to_LibreTexts_for_New_Instructors/08%3A_Meta_Information/8.03%3A_Adding_Authorbars_(Meta-Tags)A Quick-Edit tutorial on how to add authorbars in the LibreText platform.
- https://chem.libretexts.org/Courses/can/CHEM_232_-_Organic_Chemistry_II_(Puenzo)/05%3A_Aldehydes_and_Ketones-_Nucleophilic_Addition_Reactions/5.05%3A_Nucleophilic_Addition_Reactions_of_Aldehydes_and_KetonesA third way to illustrate the carbon-oxygen dipole is to consider the two main resonance contributors of a carbonyl group: the major form, which is what you typically see drawn in Lewis structures, an...A third way to illustrate the carbon-oxygen dipole is to consider the two main resonance contributors of a carbonyl group: the major form, which is what you typically see drawn in Lewis structures, and a minor but very important contributor in which both electrons in the pi bond are localized on the oxygen, giving it a full negative charge.
- https://chem.libretexts.org/Bookshelves/Organic_Chemistry/Organic_Chemistry_(Morsch_et_al.)/07%3A_Alkenes-_Structure_and_Reactivity/7.04%3A_Naming_AlkenesAlkenes contain carbon-carbon double bonds and are unsaturated hydrocarbons with the molecular formula is CnH2n; this is also the same molecular formula as cycloalkanes. For straight chain alkenes, it...Alkenes contain carbon-carbon double bonds and are unsaturated hydrocarbons with the molecular formula is CnH2n; this is also the same molecular formula as cycloalkanes. For straight chain alkenes, it is the same basic rules as nomenclature of alkanes except change the suffix to "-ene."
- https://chem.libretexts.org/Courses/can/CHEM_232_-_Organic_Chemistry_II_(Puenzo)/12%3A_Biomolecules-_Amino_Acids_Peptides_and_Proteins/12.06%3A_Amino_Acid_Analysis_of_PeptidesAs the solvent front passes the sample spots, the compounds in each sample are carried along at a rate which is characteristic of their functionality, size and interaction with the cellulose matrix of...As the solvent front passes the sample spots, the compounds in each sample are carried along at a rate which is characteristic of their functionality, size and interaction with the cellulose matrix of the paper. The ratio of the distance a compound moves from the baseline to the distance of the solvent front from the baseline is defined as the retardation (or retention) factor R f . Different amino acids usually have different R f 's under suitable conditions.
- https://chem.libretexts.org/Courses/Smith_College/Organic_Chemistry_(LibreTexts)/26%3A_Biomolecules-_Amino_Acids_Peptides_and_Proteins/26.07%3A_Amino_Acid_Analysis_of_PeptidesAs the solvent front passes the sample spots, the compounds in each sample are carried along at a rate which is characteristic of their functionality, size and interaction with the cellulose matrix of...As the solvent front passes the sample spots, the compounds in each sample are carried along at a rate which is characteristic of their functionality, size and interaction with the cellulose matrix of the paper. The ratio of the distance a compound moves from the baseline to the distance of the solvent front from the baseline is defined as the retardation (or retention) factor R f . Different amino acids usually have different R f 's under suitable conditions.
- https://chem.libretexts.org/Bookshelves/Organic_Chemistry/Organic_Chemistry_III_(Morsch_et_al.)/26%3A_Amino_Acids_Peptides_and_Proteins/26.06%3A_Amino_Acid_Analysis_of_PeptidesAs the solvent front passes the sample spots, the compounds in each sample are carried along at a rate which is characteristic of their functionality, size and interaction with the cellulose matrix of...As the solvent front passes the sample spots, the compounds in each sample are carried along at a rate which is characteristic of their functionality, size and interaction with the cellulose matrix of the paper. The ratio of the distance a compound moves from the baseline to the distance of the solvent front from the baseline is defined as the retardation (or retention) factor R f . Different amino acids usually have different R f 's under suitable conditions.
- https://chem.libretexts.org/Bookshelves/Organic_Chemistry/Organic_Chemistry_II_(Morsch_et_al.)/16%3A_Chemistry_of_Benzene_-_Electrophilic_Aromatic_Substitution/16.11%3A_Synthesis_of_Polysubstituted_BenzenesThe ability to plan a successful multi step synthesis of complex molecules is one of the goals of organic chemists. It requires a working knowledge of the uses and limitations of many organic reaction...The ability to plan a successful multi step synthesis of complex molecules is one of the goals of organic chemists. It requires a working knowledge of the uses and limitations of many organic reactions - not only which reactions to use, but when. A few examples follow:
- https://chem.libretexts.org/Bookshelves/Organic_Chemistry/Organic_Chemistry_(Morsch_et_al.)/16%3A_Chemistry_of_Benzene_-_Electrophilic_Aromatic_Substitution/16.11%3A_Synthesis_of_Polysubstituted_BenzenesThe ability to plan a successful multi step synthesis of complex molecules is one of the goals of organic chemists. It requires a working knowledge of the uses and limitations of many organic reaction...The ability to plan a successful multi step synthesis of complex molecules is one of the goals of organic chemists. It requires a working knowledge of the uses and limitations of many organic reactions - not only which reactions to use, but when. A few examples follow:
