1.1 / January 6, 2017
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Description

Organic Chemistry (Basic Reaction Mechanism) is a useful App forlearning the Basic Reaction Mechanism in organic chemistry by usingcurved arrows. Mastering the fundamentals of reaction mechanisms isan important survival skill for students learning organicchemistry. Table of Contents (Total 106 videos) 1. Types of arrowsused in organic chemistry 2. Basic principles in organic chemistry3. Resonance 4. Halogenation of alkanes (Radical reaction) 5.Alkene addition reactions: Electrophilic additions 5-1. Addition ofhydrogen halide 5-2. Stability of carbocations 5-3. Supplementary:Rearrangement reaction 5-4. Acid catalyzed addition of water(Hydration) 5-4. Reaction mechanism (How to draw curved arrows)5-5. Oxymercuration 5-6. Hydroboration 5-7. Addition of halogen(Halogenation): Bromination 5-8. Reaction with peroxyacid(peracid): Epoxidation 5-9. Reaction with osmium tetroxide:Dihydroxidation 5-10. Reaction with ozone: Ozonolysis 5-11.Reaction with hydrogen (Catalytic hydrogenation) 6. Alkyne additionreactions: Electrophilic addition 6-1. Addition of hydrogen halide6-2. Addition of water 6-3. Addition of halogen (Bromination) 6-4.Addition of hydrogen: Half reduction 6-5. Supplementary: Birchreduction 7. Electrophilic aromatic substitution 7-1. Nitration7-2. Bromination 7-3. Sulfonation: Sulfonation is reversible ! 7-4.Friedel-Crafts reactions 7-4. (A) Friedel-Crafts alkylation 7-4.(B) Friedel-Crafts acylation 7-5. Summary of electrophilic aromaticsubstitution 7-6. Electrophilic substitution of benzene derivatives7-6-1. Reactivity 7-6-2. Orientation 7-7. Theory of orientation7-7-1. Toluene: o,p-directing and activating 7-7-2. Phenol:o,p-directing and activating 7-7-3. Nitrobenzene: m-directing anddeactivating 8. Nucleophilic substitution (SN2 and SN1) of alkylhalides 8-1. SN2 reaction 8-2. Reaction mechanism of SN2 8-3. SN1reaction 8-4. Reaction mechanism of SN1 9. Elimination reaction (E2and E1) of alkyl halides 9-1. E2 reaction 9-2. Reaction mechanismof E2 9-3. E1 reaction 9-4. Reaction mechanism of E1 10. Reactionof alcohols 10-1. Protonation with strong acids 10-2.Acid-catalyzed elimination of water (Dehydration) 10-3. Reactionwith hydrogen halides 10-4. Reaction of allylic alcohols 10-5.Supplementary: Allyllic rearrangement 10-6. Supplementary:Saytzeff’s rule (Zaitsev’s rule) 11. Ethers: Synthesis andReactions 11-1. Synthesis of ethers-1 11-2. Synthesis of ethers-2:Williamson Ether Synthesis 11-3. Acid cleavage of ethers: Reactionwith acids 11-4. Supplementary: Removal of methyl protecting group11-5. Nucleophilic opening of epoxides with Grignard reagents 12.Nucleophilic addition to carbonyl group (aldehydes and ketones)12-1. The polarity of the C=O double bond 12-2. Nucleophilicaddition to carbonyl group 12-3. Addition of alcohols: Hemiacetaland acetal formation 12-4. Addition of primary amines: Imineformation 12-5. Addition of Grignard reagents 12-6. Supplementary:Addition of Grignard reagents to carbon dioxide 12-7. Addition ofacetylides 12-8. Addition of hydrogen cyanide 12-9. Reduction ofketones and aldehydes 13. Esters: Synthesis and Reactions 13-1.Synthetic method for esters-1: Fischer esterification 13-2.Synthetic method for esters-2: Methyl ester formation bydiazomethane 13-3. Hydrolysis of esters 13-4. Supplementary:Acid-catalyzed hydrolysis of tert-butyl esters 13-5. Reaction withGrignard reagents 13-6. Reduction of esters 13-7. Alcoholysis ofesters 13-8. Ammonolysis of esters 14. Enol and Enolate reactions(aldehydes and ketones) 14-1. Keto-enol equilibrium 14-2. Why area-Hydrogens acidic ? 14-3. Enolization 14-4. Aldol reaction 14-5.Aldol condensation 14-6. E1cB reaction 15. Enolate reactions inesters 15-1. Claisen condensation 15-2. Dieckmann condensation andretro-Claisen condensation 15-3. Synthetic methods related toClaisen condensation 15-4. Acetoacetic ester synthesis 15-5.Malonic ester synthesis 16. Michael addition 17. Robinsonannulation

App Information Organic Chemistry

  • App Name
    Organic Chemistry
  • Package Name
    appinventor.ai_yfd51885.OrganicChemistry_e
  • Updated
    January 6, 2017
  • File Size
    32M
  • Requires Android
    Android 2.3 and up
  • Version
    1.1
  • Developer
    YOSHITAKA MATSUSHIMA
  • Installs
    10+
  • Price
    $4.99
  • Category
    Education
  • Developer
    〒156-8502 世田谷区桜丘1-1-1東京農業大学・農芸化学科
  • Google Play Link

YOSHITAKA MATSUSHIMA Show More...

Organic Chemistry Japanese ver 1.0 APK
Organic Chemistry English ver. is a usefulAppfor learning the fundamentals of reaction mechanism inorganicchemistry by using curved arrows. Mastering the fundamentalsofreaction mechanisms is an important survival skill forstudentslearning organic chemistry.A Selected Table of Contents (Total 106 videos)1. Types of arrows used in organic chemistry2. Basic principles in organic chemistry3. Resonance4. Halogenation of alkanes (Radical reaction)5. Alkene addition reactions: Electrophilic additions 5-1.Additionof hydrogen halide5-2. Stability of carbocations5-3. Supplementary: Rearrangement reaction5-4. Acid catalyzed addition of water (Hydration)5-4. Reaction mechanism (How to draw curved arrows)5-5. Oxymercuration5-6. Hydroboration5-7. Addition of halogen (Halogenation): Bromination5-8. Reaction with peroxyacid (peracid): Epoxidation 5-9.Reactionwith osmium tetroxide: Dihydroxidation5-10. Reaction with ozone: Ozonolysis5-11. Reaction with hydrogen (Catalytic hydrogenation)6. Alkyne addition reactions: Electrophilic addition 6-1.Additionof hydrogen halide6-2. Addition of water6-3. Addition of halogen (Bromination) 6-4. Addition ofhydrogen:Half reduction6-5. Supplementary: Birch reduction7. Electrophilic aromatic substitution 7-1. Nitration7-2. Bromination7-3. Sulfonation: Sulfonation is reversible !7-4. Friedel-Crafts reactions 7-4. (A)Friedel-Craftsalkylation7-4. (B) Friedel-Crafts acylation7-5. Summary of electrophilic aromatic substitution7-6. Electrophilic substitution of benzene derivatives7-6-1.Reactivity7-6-2. Orientation7-7. Theory of orientation 7-7-1. Toluene: o,p-directingandactivating7-7-2. Phenol: o,p-directing and activating7-7-3. Nitrobenzene: m-directing and deactivating8. Nucleophilic substitution (SN2 and SN1) of alkyl halides 8-1.SN2reaction8-2. Reaction mechanism of SN28-3. SN1 reaction8-4. Reaction mechanism of SN19. Elimination reaction (E2 and E1) of alkyl halides 9-1.E2reaction9-2. Reaction mechanism of E29-3. E1 reaction9-4. Reaction mechanism of E110. Reaction of alcohols 10-1. Protonation with strong acids10-2. Acid-catalyzed elimination of water (Dehydration)10-3. Reaction with hydrogen halides10-4. Reaction of allylic alcohols10-5. Supplementary: Allyllic rearrangement10-6. Supplementary: Saytzeff’s rule (Zaitsev’s rule)11. Ethers: Synthesis and Reactions 11-1. Synthesis ofethers-111-2. Synthesis of ethers-2: Williamson EtherSynthesis11-3. Acid cleavage of ethers: Reaction with acids11-4. Supplementary: Removal of methyl protecting group11-5. Nucleophilic opening of epoxides with Grignard reagents12. Nucleophilic addition to carbonyl group (aldehydes andketones)12-1. The polarity of the C=O double bond12-2. Nucleophilic addition to carbonyl group12-3. Addition of alcohols: Hemiacetal and acetal formation12-4. Addition of primary amines: Imine formation12-5. Addition of Grignard reagents12-6. Supplementary: Addition of Grignard reagents tocarbondioxide12-7. Addition of acetylides12-8. Addition of hydrogen cyanide12-9. Reduction of ketones and aldehydes13. Esters: Synthesis and Reactions 13-1. Synthetic methodforesters-1: Fischer esterification13-2. Synthetic method for esters-2: Methyl ester formationbydiazomethane13-3. Hydrolysis of esters13-4. Supplementary: Acid-catalyzed hydrolysis oftert-butylesters13-5. Reaction with Grignard reagents13-6. Reduction of esters13-7. Alcoholysis of esters 13-8. Ammonolysis of esters14. Enol and Enolate reactions (aldehydes and ketones)14-1.Keto-enol equilibrium14-2. Why are a-Hydrogens acidic ?14-3. Enolization14-4. Aldol reaction14-5. Aldol condensation14-6. E1cB reaction15. Enolate reactions in esters 15-1. Claisen condensation15-2. Dieckmann condensation and retro-Claisen condensation15-3. Synthetic methods related to Claisen condensation15-4. Acetoacetic ester synthesis15-5. Malonic ester synthesis16. Michael addition17. Robinson annulation
Organic Chemistry 1.1 APK
Organic Chemistry (Basic Reaction Mechanism) is a useful App forlearning the Basic Reaction Mechanism in organic chemistry by usingcurved arrows. Mastering the fundamentals of reaction mechanisms isan important survival skill for students learning organicchemistry. Table of Contents (Total 106 videos) 1. Types of arrowsused in organic chemistry 2. Basic principles in organic chemistry3. Resonance 4. Halogenation of alkanes (Radical reaction) 5.Alkene addition reactions: Electrophilic additions 5-1. Addition ofhydrogen halide 5-2. Stability of carbocations 5-3. Supplementary:Rearrangement reaction 5-4. Acid catalyzed addition of water(Hydration) 5-4. Reaction mechanism (How to draw curved arrows)5-5. Oxymercuration 5-6. Hydroboration 5-7. Addition of halogen(Halogenation): Bromination 5-8. Reaction with peroxyacid(peracid): Epoxidation 5-9. Reaction with osmium tetroxide:Dihydroxidation 5-10. Reaction with ozone: Ozonolysis 5-11.Reaction with hydrogen (Catalytic hydrogenation) 6. Alkyne additionreactions: Electrophilic addition 6-1. Addition of hydrogen halide6-2. Addition of water 6-3. Addition of halogen (Bromination) 6-4.Addition of hydrogen: Half reduction 6-5. Supplementary: Birchreduction 7. Electrophilic aromatic substitution 7-1. Nitration7-2. Bromination 7-3. Sulfonation: Sulfonation is reversible ! 7-4.Friedel-Crafts reactions 7-4. (A) Friedel-Crafts alkylation 7-4.(B) Friedel-Crafts acylation 7-5. Summary of electrophilic aromaticsubstitution 7-6. Electrophilic substitution of benzene derivatives7-6-1. Reactivity 7-6-2. Orientation 7-7. Theory of orientation7-7-1. Toluene: o,p-directing and activating 7-7-2. Phenol:o,p-directing and activating 7-7-3. Nitrobenzene: m-directing anddeactivating 8. Nucleophilic substitution (SN2 and SN1) of alkylhalides 8-1. SN2 reaction 8-2. Reaction mechanism of SN2 8-3. SN1reaction 8-4. Reaction mechanism of SN1 9. Elimination reaction (E2and E1) of alkyl halides 9-1. E2 reaction 9-2. Reaction mechanismof E2 9-3. E1 reaction 9-4. Reaction mechanism of E1 10. Reactionof alcohols 10-1. Protonation with strong acids 10-2.Acid-catalyzed elimination of water (Dehydration) 10-3. Reactionwith hydrogen halides 10-4. Reaction of allylic alcohols 10-5.Supplementary: Allyllic rearrangement 10-6. Supplementary:Saytzeff’s rule (Zaitsev’s rule) 11. Ethers: Synthesis andReactions 11-1. Synthesis of ethers-1 11-2. Synthesis of ethers-2:Williamson Ether Synthesis 11-3. Acid cleavage of ethers: Reactionwith acids 11-4. Supplementary: Removal of methyl protecting group11-5. Nucleophilic opening of epoxides with Grignard reagents 12.Nucleophilic addition to carbonyl group (aldehydes and ketones)12-1. The polarity of the C=O double bond 12-2. Nucleophilicaddition to carbonyl group 12-3. Addition of alcohols: Hemiacetaland acetal formation 12-4. Addition of primary amines: Imineformation 12-5. Addition of Grignard reagents 12-6. Supplementary:Addition of Grignard reagents to carbon dioxide 12-7. Addition ofacetylides 12-8. Addition of hydrogen cyanide 12-9. Reduction ofketones and aldehydes 13. Esters: Synthesis and Reactions 13-1.Synthetic method for esters-1: Fischer esterification 13-2.Synthetic method for esters-2: Methyl ester formation bydiazomethane 13-3. Hydrolysis of esters 13-4. Supplementary:Acid-catalyzed hydrolysis of tert-butyl esters 13-5. Reaction withGrignard reagents 13-6. Reduction of esters 13-7. Alcoholysis ofesters 13-8. Ammonolysis of esters 14. Enol and Enolate reactions(aldehydes and ketones) 14-1. Keto-enol equilibrium 14-2. Why area-Hydrogens acidic ? 14-3. Enolization 14-4. Aldol reaction 14-5.Aldol condensation 14-6. E1cB reaction 15. Enolate reactions inesters 15-1. Claisen condensation 15-2. Dieckmann condensation andretro-Claisen condensation 15-3. Synthetic methods related toClaisen condensation 15-4. Acetoacetic ester synthesis 15-5.Malonic ester synthesis 16. Michael addition 17. Robinsonannulation
有機化学 Organic Chemistry 基本の反応機構 1.0 APK

有機化学の基本反応について、巻矢印を使った反応機構を理解し、自分で書けるようになるための学習用アプリ。
それが『有機化学Organic Chemistry 基本の反応機構』です。『有機化学 Organic Chemistry基本の反応機構』は、大学の1〜2年時の学習や、その後の専門課程における学習や研究において重要な有機化学の基礎知識の習得に役立ちます。高校で有機化学をしっかり学習した人なら、大学の有機化学の入門としての勉強に最適です。
◎ 主な内容
1.有機化学における矢印の意味と書き方
2.有機化学反応の基礎的事項について
3.共鳴
4.アルカンのハロゲン化(ラジカル反応)
5.アルケンの反応: 求電子付加反応
6.アルキンの反応:求電子付加反応
7.求電子芳香族置換反応
8.求核置換反応(ハロゲン化アルキル):SN2とSN1反応など
9.脱離反応(ハロゲン化アルキル):E2とE1反応など
10.アルコールの反応
11.エーテルに関する反応
12.カルボニル基への求核付加反応(アルデヒド・ケトン)
13.エステルに関する反応:Fischer のエステル化や加水分解など
14.エノール・エノラートアニオンの関与する反応(アルデヒド・ケトン):アルドール反応(縮合)など
15.エノラートアニオンの関与する反応(エステル):Claisen縮合など
16.Michael付加
17.Robinson成環反応



【機能・使い方】
1.アプリを立ちあげると全内容の目次が表示されます。各項目をタップすると内容が自動的に動画再生されます。
2.電子の動きを示す巻矢印が動画で表示され、その結果生じる化合物の化学構造式が表示されます。
3.画面をタップすると、シーク機能により任意の位置から動画を再生できますので、繰り返し学習に効果的です。4.戻るボタンや画面の右スワイプで目次に戻ることができます。
【その他注意事項】
<アプリ内容の訂正>
項目7−2.でBr+をbromonium ionとしているのは間違いです。haloniumionは、アルケンへのハロゲンの付加の中間体など、一般式 R-X+-R' の名称です。<アプリの内容に関する情報>アプリの内容や使い方などに関する補足情報をTwitter(http://twitter.com/organic_chemist)で流しています。質問も受け付けることもできます。
Organic Chemistry Eng/Jap (for 1.0 APK
App for learning the reaction mechanism in organic chemistry bycurved arrows.
Organic Chemistry 1.1 APK
App for learning the reaction mechanism in organic chemistry bycurved arrows.