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- https://chem.libretexts.org/Courses/Williams_School/Advanced_Chemistry/11%3A_An_Overview_of_Organic_Reactions/11.03%3A_Polar_ReactionsThe resonance of the carbon partial positive charge allows the negative charge on the nucleophile to attack the Carbonyl group and become a part of the structure and a positive charge (usually a proto...The resonance of the carbon partial positive charge allows the negative charge on the nucleophile to attack the Carbonyl group and become a part of the structure and a positive charge (usually a proton hydrogen) attacks the oxygen.
- https://chem.libretexts.org/Bookshelves/Organic_Chemistry/Organic_Chemistry_I_(Morsch_et_al.)/06%3A_An_Overview_of_Organic_Reactions/6.04%3A_Polar_ReactionsThe resonance of the carbon partial positive charge allows the negative charge on the nucleophile to attack the Carbonyl group and become a part of the structure and a positive charge (usually a proto...The resonance of the carbon partial positive charge allows the negative charge on the nucleophile to attack the Carbonyl group and become a part of the structure and a positive charge (usually a proton hydrogen) attacks the oxygen.
- https://chem.libretexts.org/Workbench/LCDS_Organic_Chemistry_OER_Textbook_-_Todd_Trout/06%3A_An_Overview_of_Organic_Reactions/6.03%3A_How_Organic_Reactions_Occur_-_MechanismsWe’ll develop this point in more detail later, but note for now that the movement of two electrons in the unsymmetrical process is indicated using a full-headed curved arrow ( ), whereas the movement ...We’ll develop this point in more detail later, but note for now that the movement of two electrons in the unsymmetrical process is indicated using a full-headed curved arrow ( ), whereas the movement of one electron in the symmetrical process is indicated using a half-headed, or “fishhook,” arrow ( ).
- https://chem.libretexts.org/Bookshelves/Organic_Chemistry/Organic_Chemistry_(OpenStax)/06%3A_An_Overview_of_Organic_Reactions/6.03%3A_Polar_ReactionsPolar reactions occur because of the electrical attraction between positively polarized and negatively polarized centers on functional groups in molecules. Most organic compounds are electrically neut...Polar reactions occur because of the electrical attraction between positively polarized and negatively polarized centers on functional groups in molecules. Most organic compounds are electrically neutral; they have no net charge, either positive or negative. However, certain bonds within a molecule, particularly the bonds in functional groups, are polar, which is a consequence of an unsymmetrical electron distribution in a bond due to the difference in electronegativity of the bonded atoms.
- https://chem.libretexts.org/Courses/can/CHEM_231%3A_Organic_Chemistry_I_Textbook/06%3A_An_Overview_of_Organic_Reactions/6.05%3A_Polar_ReactionsA nucleophile is a substance that is “nucleus-loving.” (Remember that a nucleus is positively charged.) A nucleophile has a negatively polarized, electron-rich atom and can form a bond by donating a p...A nucleophile is a substance that is “nucleus-loving.” (Remember that a nucleus is positively charged.) A nucleophile has a negatively polarized, electron-rich atom and can form a bond by donating a pair of electrons to a positively polarized, electron-poor atom.
- https://chem.libretexts.org/Courses/can/CHEM_231%3A_Organic_Chemistry_I_Textbook/06%3A_An_Overview_of_Organic_Reactions/6.03%3A_How_Organic_Reactions_Occur_-_MechanismsWe’ll develop this point in more detail later, but note for now that the movement of two electrons in the unsymmetrical process is indicated using a full-headed curved arrow ( ), whereas the movement ...We’ll develop this point in more detail later, but note for now that the movement of two electrons in the unsymmetrical process is indicated using a full-headed curved arrow ( ), whereas the movement of one electron in the symmetrical process is indicated using a half-headed, or “fishhook,” arrow ( ).
- https://chem.libretexts.org/Courses/Chandler_Gilbert_Community_College/Fundamental_Organic_ala_Mech/05%3A_Unit_2/5.02%3A_Reactions_overview/5.2.04%3A_Polar_ReactionsA nucleophile is a substance that is “nucleus-loving.” (Remember that a nucleus is positively charged.) A nucleophile has a negatively polarized, electron-rich atom and can form a bond by donating a p...A nucleophile is a substance that is “nucleus-loving.” (Remember that a nucleus is positively charged.) A nucleophile has a negatively polarized, electron-rich atom and can form a bond by donating a pair of electrons to a positively polarized, electron-poor atom.
- https://chem.libretexts.org/Bookshelves/Organic_Chemistry/Organic_Chemistry_(Morsch_et_al.)/06%3A_An_Overview_of_Organic_Reactions/6.02%3A_How_Organic_Reactions_Occur_-_MechanismsThe ending of the word tells you whether a bond is being formed (‑genic) or broken (‑lytic), while the root of the word describes the nature of that formation or decomposition. The importance of elect...The ending of the word tells you whether a bond is being formed (‑genic) or broken (‑lytic), while the root of the word describes the nature of that formation or decomposition. The importance of electrophile / nucleophile terminology comes from the fact that many organic reactions involve at some stage the bonding of a nucleophile to an electrophile, a process that generally leads to a stable intermediate or product.
- https://chem.libretexts.org/Courses/Smith_College/Organic_Chemistry_(LibreTexts)/06%3A_An_Overview_of_Organic_Reactions/6.03%3A_How_Organic_Reactions_Occur_-_MechanismsThe ending of the word tells you whether a bond is being formed (‑genic) or broken (‑lytic), while the root of the word describes the nature of that formation or decomposition. The importance of elect...The ending of the word tells you whether a bond is being formed (‑genic) or broken (‑lytic), while the root of the word describes the nature of that formation or decomposition. The importance of electrophile / nucleophile terminology comes from the fact that many organic reactions involve at some stage the bonding of a nucleophile to an electrophile, a process that generally leads to a stable intermediate or product.
- https://chem.libretexts.org/Courses/Chandler_Gilbert_Community_College/Fundamental_Organic_ala_Mech/05%3A_Unit_2/5.02%3A_Reactions_overview/5.2.03%3A_How_Organic_Reactions_Occur_-_MechanismsWe’ll develop this point in more detail later, but note for now that the movement of two electrons in the unsymmetrical process is indicated using a full-headed curved arrow ( ), whereas the movement ...We’ll develop this point in more detail later, but note for now that the movement of two electrons in the unsymmetrical process is indicated using a full-headed curved arrow ( ), whereas the movement of one electron in the symmetrical process is indicated using a half-headed, or “fishhook,” arrow ( ).
- https://chem.libretexts.org/Courses/Smith_College/Organic_Chemistry_(LibreTexts)/06%3A_An_Overview_of_Organic_Reactions/6.05%3A_Polar_ReactionsThe resonance of the carbon partial positive charge allows the negative charge on the nucleophile to attack the Carbonyl group and become a part of the structure and a positive charge (usually a proto...The resonance of the carbon partial positive charge allows the negative charge on the nucleophile to attack the Carbonyl group and become a part of the structure and a positive charge (usually a proton hydrogen) attacks the oxygen.
