[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"skill:01M6HA8M1VXZ4S8CP72CDHNVC6":3,"skill-same:01M6HA8M1VXZ4S8CP72CDHNVC6":54},{"skillNo":4,"name":5,"nameZh":6,"description":7,"descriptionZh":6,"repositoryFullName":8,"ownerLogin":9,"ownerAvatarUrl":10,"ownerAccountNo":11,"ownerDisplayName":12,"repositoryNo":13,"starsCount":14,"licenseSpdxId":15,"licenseFileUrl":6,"sourceHtmlUrl":16,"categories":17,"keywords":18,"publishedAt":24,"linkOnly":25,"markdownContent":26,"markdownBody":27,"frontMatter":28,"refName":32,"commitSha":33,"skillDirectory":34,"forksCount":14,"repositoryHtmlUrl":35,"repositoryHomepageUrl":6,"ownerHtmlUrl":36,"ownerBlogUrl":37,"ownerDescription":38,"updatedAt":39,"install":40,"resources":53},"01M6HA8M1VXZ4S8CP72CDHNVC6","organic-chemistry",null,"Chemistry of carbon compounds","NeuralBlitz\u002FMito","NeuralBlitz","https:\u002F\u002Favatars.githubusercontent.com\u002Fu\u002F79354388?v=4","01M6H8T2TFH477HRS0KTSTKR2E","David 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Functional Groups\n\n| Class | Structure | Example |\n|-------|-----------|---------|\n| Alkane | C-H, C-C | CH₄ |\n| Alkene | C=C | C₂H₄ |\n| Alkyne | C≡C | C₂H₂ |\n| Alcohol | -OH | C₂H₅OH |\n| Ether | R-O-R' | diethyl ether |\n| Aldehyde | -CHO | CH₃CHO |\n| Ketone | R-CO-R' | acetone |\n| Carboxylic acid | -COOH | acetic acid |\n| Amine | -NH₂ | ethylamine |\n\n### Reaction Mechanisms\n\n```python\n# Example: SN1 vs SN2 reaction analysis\ndef reaction_type(substrate, nucleophile, solvent):\n    \"\"\"\n    Determine likely mechanism.\n    \"\"\"\n    # SN2: Primary alkyl halide, strong nucleophile, polar aprotic\n    if substrate in ['methyl', 'primary'] and nucleophile == 'strong':\n        return 'SN2'\n    \n    # SN1: Tertiary alkyl halide, weak nucleophile, polar protic\n    elif substrate == 'tertiary' and nucleophile == 'weak':\n        return 'SN1'\n    \n    # E2: Strong base, anti-periplanar H\n    elif nucleophile == 'strong_base':\n        return 'E2'\n    \n    return 'mixture'\n```\n\n### Stereochemistry\n\n- Chiral centers\n- Enantiomers vs diastereomers\n- R\u002FS configuration\n- E\u002FZ isomerism (alkenes)\n- Meso compounds\n- Optical activity\n\n### Synthesis Strategies\n\n- Retrosynthetic analysis\n- Functional group transformations\n- Protecting groups\n- Carbon-carbon bond formation\n- Oxidation\u002Freduction\n- Stereocontrol\n","## What I do\n\n- Study carbon-based compounds and reactions\n- Analyze organic reaction mechanisms\n- Design synthetic routes\n- Characterize organic molecules\n- Investigate stereochemistry\n- Develop new synthetic methods\n\n## When to use me\n\n- When studying organic reactions\n- When designing syntheses\n- When analyzing mechanisms\n- When working with functional groups\n- When determining stereochemistry\n- When characterizing organic compounds\n\n## Key Concepts\n\n### Functional Groups\n\n| Class | Structure | Example |\n|-------|-----------|---------|\n| Alkane | C-H, C-C | CH₄ |\n| Alkene | C=C | C₂H₄ |\n| Alkyne | C≡C | C₂H₂ |\n| Alcohol | -OH | C₂H₅OH |\n| Ether | R-O-R' | diethyl ether |\n| Aldehyde | -CHO | CH₃CHO |\n| Ketone | R-CO-R' | acetone |\n| Carboxylic acid | -COOH | acetic acid |\n| Amine | -NH₂ | ethylamine |\n\n### Reaction Mechanisms\n\n```python\n# Example: SN1 vs SN2 reaction analysis\ndef reaction_type(substrate, nucleophile, solvent):\n    \"\"\"\n    Determine likely mechanism.\n    \"\"\"\n    # SN2: Primary alkyl halide, strong nucleophile, polar aprotic\n    if substrate in ['methyl', 'primary'] and nucleophile == 'strong':\n        return 'SN2'\n    \n    # SN1: Tertiary alkyl halide, weak nucleophile, polar protic\n    elif substrate == 'tertiary' and nucleophile == 'weak':\n        return 'SN1'\n    \n    # E2: Strong base, anti-periplanar H\n    elif nucleophile == 'strong_base':\n        return 'E2'\n    \n    return 'mixture'\n```\n\n### Stereochemistry\n\n- Chiral centers\n- Enantiomers vs diastereomers\n- R\u002FS configuration\n- E\u002FZ isomerism 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