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- https://chem.libretexts.org/Courses/Oregon_Institute_of_Technology/OIT_(Lund)%3A_Organic_Chemistry_with_a_Biological_Emphasis_(Soderberg)/07%3A_Acid-base_Reactions/7.06%3A_Carbon_AcidsSo far, we have limited our discussion of acidity and basicity to heteroatom acids, where the acidic proton is bound to an oxygen, nitrogen, sulfur, or halogen. However, carbon acids - in which the pr...So far, we have limited our discussion of acidity and basicity to heteroatom acids, where the acidic proton is bound to an oxygen, nitrogen, sulfur, or halogen. However, carbon acids - in which the proton to be donated is bonded to a carbon atom - play an integral role in biochemistry.
- https://chem.libretexts.org/Courses/Oregon_Institute_of_Technology/OIT_(Lund)%3A_Organic_Chemistry_with_a_Biological_Emphasis_(Soderberg)/11%3A_Nucleophilic_Acyl_Substitution_Reactions/11.10%3A_A_Look_Ahead_-_Acyl_Substitution_Reactions_with_a_Carbanion_or_Hydride_Ion_NucleophileAlthough we have seen many different types of nucleophilic acyl substitutions in this chapter, we have not yet encountered a reaction in which the incoming nucleophile is a carbanion or a hydride. Rec...Although we have seen many different types of nucleophilic acyl substitutions in this chapter, we have not yet encountered a reaction in which the incoming nucleophile is a carbanion or a hydride. Recall that in the previous chapter on aldehydes and ketones, we also postponed discussion of nucleophilic carbonyl addition reactions in which a carbanion or a hydride is the nucleophile.
- https://chem.libretexts.org/Ancillary_Materials/Reference/Organic_Chemistry_Glossary/CarbanionThe removal of a hydrogen atom on a carbon atom in an organic molecule as a proton results in a species that has a formal charge of -1 on a carbon atom. It is called a carbanion.
- https://chem.libretexts.org/Courses/SUNY_Oneonta/Organic_Chemistry_with_a_Biological_Emphasis_(SUNY_Oneonta)/07%3A_Acid-base_Reactions/7.07%3A_Carbon_AcidsSo far, we have limited our discussion of acidity and basicity to heteroatom acids, where the acidic proton is bound to an oxygen, nitrogen, sulfur, or halogen. However, carbon acids - in which the pr...So far, we have limited our discussion of acidity and basicity to heteroatom acids, where the acidic proton is bound to an oxygen, nitrogen, sulfur, or halogen. However, carbon acids - in which the proton to be donated is bonded to a carbon atom - play an integral role in biochemistry.
- https://chem.libretexts.org/Bookshelves/Introductory_Chemistry/Introduction_to_Organic_and_Biochemistry_(Malik)/01%3A_Bonding_in_organic_compounds/1.05%3A_Formal_ChargeA formal charge is assigned to an atom in a molecule based on the assumption that bonding electrons are shared equally. Calculating formal charges and characteristics of some organic species having fo...A formal charge is assigned to an atom in a molecule based on the assumption that bonding electrons are shared equally. Calculating formal charges and characteristics of some organic species having formal charges are described.
- https://chem.libretexts.org/Bookshelves/Organic_Chemistry/Book%3A_Organic_Chemistry_with_a_Biological_Emphasis_v2.0_(Soderberg)/11%3A_Nucleophilic_Acyl_Substitution_Reactions/11.11%3A_A_Look_Ahead_-_Acyl_Substitution_Reactions_with_a_Carbanion_or_Hydride_Ion_NucleophileAlthough we have seen many different types of nucleophilic acyl substitutions in this chapter, we have not yet encountered a reaction in which the incoming nucleophile is a carbanion or a hydride. Rec...Although we have seen many different types of nucleophilic acyl substitutions in this chapter, we have not yet encountered a reaction in which the incoming nucleophile is a carbanion or a hydride. Recall that in the previous chapter on aldehydes and ketones, we also postponed discussion of nucleophilic carbonyl addition reactions in which a carbanion or a hydride is the nucleophile.
- https://chem.libretexts.org/Courses/Oregon_Institute_of_Technology/OIT%3A_CHE_332_--_Organic_Chemistry_II_(Lund)/7%3A_Acid-base_Reactions/7.6%3A_Carbon_AcidsSo far, we have limited our discussion of acidity and basicity to heteroatom acids, where the acidic proton is bound to an oxygen, nitrogen, sulfur, or halogen. However, carbon acids - in which the pr...So far, we have limited our discussion of acidity and basicity to heteroatom acids, where the acidic proton is bound to an oxygen, nitrogen, sulfur, or halogen. However, carbon acids - in which the proton to be donated is bonded to a carbon atom - play an integral role in biochemistry.
- https://chem.libretexts.org/Courses/Oregon_Institute_of_Technology/OIT%3A_CHE_333_-_Organic_Chemistry_III_(Lund)/New_Page/7%3A_Acid-base_Reactions/7.6%3A_Carbon_AcidsSo far, we have limited our discussion of acidity and basicity to heteroatom acids, where the acidic proton is bound to an oxygen, nitrogen, sulfur, or halogen. However, carbon acids - in which the pr...So far, we have limited our discussion of acidity and basicity to heteroatom acids, where the acidic proton is bound to an oxygen, nitrogen, sulfur, or halogen. However, carbon acids - in which the proton to be donated is bonded to a carbon atom - play an integral role in biochemistry.
- https://chem.libretexts.org/Courses/SUNY_Oneonta/Organic_Chemistry_with_a_Biological_Emphasis_(SUNY_Oneonta)/11%3A_Nucleophilic_Acyl_Substitution_Reactions/11.11%3A_A_Look_Ahead_-_Acyl_Substitution_Reactions_with_a_Carbanion_or_Hydride_Ion_NucleophileAlthough we have seen many different types of nucleophilic acyl substitutions in this chapter, we have not yet encountered a reaction in which the incoming nucleophile is a carbanion or a hydride. Rec...Although we have seen many different types of nucleophilic acyl substitutions in this chapter, we have not yet encountered a reaction in which the incoming nucleophile is a carbanion or a hydride. Recall that in the previous chapter on aldehydes and ketones, we also postponed discussion of nucleophilic carbonyl addition reactions in which a carbanion or a hydride is the nucleophile.
- https://chem.libretexts.org/Courses/Oregon_Institute_of_Technology/OIT%3A_CHE_332_--_Organic_Chemistry_II_(Lund)/11%3A_Nucleophilic_Acyl_Substitution_Reactions/11.Z%3A_A_Look_Ahead_-_Acyl_Substitution_Reactions_with_a_Carbanion_or_Hydride_Ion_NucleophileAlthough we have seen many different types of nucleophilic acyl substitutions in this chapter, we have not yet encountered a reaction in which the incoming nucleophile is a carbanion or a hydride. Rec...Although we have seen many different types of nucleophilic acyl substitutions in this chapter, we have not yet encountered a reaction in which the incoming nucleophile is a carbanion or a hydride. Recall that in the previous chapter on aldehydes and ketones, we also postponed discussion of nucleophilic carbonyl addition reactions in which a carbanion or a hydride is the nucleophile.
- https://chem.libretexts.org/Bookshelves/Organic_Chemistry/Book%3A_Organic_Chemistry_with_a_Biological_Emphasis_v2.0_(Soderberg)/07%3A_Acid-base_Reactions/7.07%3A_Carbon_AcidsSo far, we have limited our discussion of acidity and basicity to heteroatom acids, where the acidic proton is bound to an oxygen, nitrogen, sulfur, or halogen. However, carbon acids - in which the pr...So far, we have limited our discussion of acidity and basicity to heteroatom acids, where the acidic proton is bound to an oxygen, nitrogen, sulfur, or halogen. However, carbon acids - in which the proton to be donated is bonded to a carbon atom - play an integral role in biochemistry.
