జమ్మూకశ్మీర్‌: మాచిల్‌లో చొరబాటుకు ప్రయత్నం, ఓ ఉగ్రవాదిని హతమార్చిన భారత సైన్యం|మిథాలీరాజ్‌కు బీఎండబ్ల్యూ కారు ప్రకటించిన చాముండి|విశాఖ: డ్రగ్స్ నియంత్రణపై స్కూల్ యాజమాన్యాలకు అవగాహన సమావేశం|కరీంనగర్‌: ఆర్టీసీ బస్టాండ్‌ ఆధునీకరణ పనులను ప్రారంభించిన మంత్రులు మహేందర్ రెడ్డి, ఈటల |కర్నూలు: నంద్యాలలో రెండో రోజు చంద్రబాబు పర్యటన |బంగాళాఖాతంలో మరో రెండు రోజుల్లో అల్పపీడనం |తిరుపతి: తిరుచానూరు పద్మావతి అమ్మవారిని దర్శించుకున్న మాజీ ఎంపీ లగడపాటి రాజగోపాల్‌| ఢిల్లీలో కార్గిల్‌ పరాక్రమ్‌ ర్యాలీ, పరాక్రమ్‌ ర్యాలీలో పాల్గొన్న వెంకయ్యనాయుడు| తెలంగాణలో ఒంటరిగానే పోటీ చేస్తాం: లక్ష్మణ్‌|వరంగల్: రెండో రోజు బీజేపీ రాష్ట్ర కార్యవర్గ సమావేశాలు

ఆంధ్రజ్యోతి హోం

రెజ్యూమ్‌లో ఈ 10 పదాలు వాడకపోవడమే మంచిదట..! |

ఈ 10 ప్రశ్నలకు ముందే ప్రిపేర్ అవ్వండి |

ఈ సీవీ తయారీకి 70 గంటలు |

పోటీ పరీక్షలకు ప్రిపేర్ అయే నిరుద్యోగులకు శుభవార్త |

సివిల్స్‌లో 464వ ర్యాంకర్.. ప్రత్యేక ఇంటర్వ్యూ |

జాబ్‌ అలర్ట్స్‌.. సెట్‌ చేసుకోండిలా |

Others

INTERMEDIATE - II

11 - Haloalkanes and Haloarenes

11.3.Methods of Preparation : Alkyl Halides and Aryl Halides- from Alcohols, from Hydrocarbons (a) By Free Radical Halogenations – (b) By Electrophilic Substitution (c) By replacement of Diazonium Group (Sand-Meyer Reaction) (d) By the Addition of Hydrogen Halides and Halogens to Alkenes - By Halogen Exchange (Finkelstein reaction)

Chapter : 11 - Haloalkanes and Haloarenes

Remaining lessons :

11.0. Introduction

11.1 Classification and Nomenclature

11.2 Nature of C-X Bond

11.3.Methods of Preparation : Alkyl Halides and Aryl Halides- from Alcohols, from Hydrocarbons (a) By Free Radical Halogenations – (b) By Electrophilic Substitution (c) By replacement of Diazonium Group (Sand-Meyer Reaction) (d) By the Addition of Hydrogen Halides and Halogens to Alkenes - By Halogen Exchange (Finkelstein reaction)

11.3.Methods of Preparation : Alkyl Halides and Aryl Halides- from Alcohols, from Hydrocarbons (a) By Free Radical Halogenations – (b) By Electrophilic Substitution (c) By replacement of Diazonium Group (Sand-Meyer Reaction) (d) By the Addition of Hydrogen Halides and Halogens to Alkenes - By Halogen Exchange (Finkelstein reaction)

11.3.Methods of Preparation : Alkyl Halides and Aryl Halides- from Alcohols, from Hydrocarbons (a) By Free Radical Halogenations – (b) By Electrophilic Substitution (c) By replacement of Diazonium Group (Sand-Meyer Reaction) (d) By the Addition of Hydrogen Halides and Halogens to Alkenes - By Halogen Exchange (Finkelstein reaction)

11.3.Methods of Preparation : Alkyl Halides and Aryl Halides- from Alcohols, from Hydrocarbons (a) By Free Radical Halogenations – (b) By Electrophilic Substitution (c) By replacement of Diazonium Group (Sand-Meyer Reaction) (d) By the Addition of Hydrogen Halides and Halogens to Alkenes - By Halogen Exchange (Finkelstein reaction)

11.3.Methods of Preparation : Alkyl Halides and Aryl Halides- from Alcohols, from Hydrocarbons (a) By Free Radical Halogenations – (b) By Electrophilic Substitution (c) By replacement of Diazonium Group (Sand-Meyer Reaction) (d) By the Addition of Hydrogen Halides and Halogens to Alkenes - By Halogen Exchange (Finkelstein reaction)

11.3.Methods of Preparation : Alkyl Halides and Aryl Halides- from Alcohols, from Hydrocarbons (a) By Free Radical Halogenations – (b) By Electrophilic Substitution (c) By replacement of Diazonium Group (Sand-Meyer Reaction) (d) By the Addition of Hydrogen Halides and Halogens to Alkenes - By Halogen Exchange (Finkelstein reaction)

11.3.Methods of Preparation : Alkyl Halides and Aryl Halides- from Alcohols, from Hydrocarbons (a) By Free Radical Halogenations – (b) By Electrophilic Substitution (c) By replacement of Diazonium Group (Sand-Meyer Reaction) (d) By the Addition of Hydrogen Halides and Halogens to Alkenes - By Halogen Exchange (Finkelstein reaction)

11.3.Methods of Preparation : Alkyl Halides and Aryl Halides- from Alcohols, from Hydrocarbons (a) By Free Radical Halogenations – (b) By Electrophilic Substitution (c) By replacement of Diazonium Group (Sand-Meyer Reaction) (d) By the Addition of Hydrogen Halides and Halogens to Alkenes - By Halogen Exchange (Finkelstein reaction)

11.4 Physical Properties- Melting and Boiling Points, Density and Solubility

11.4 Physical Properties- Melting and Boiling Points, Density and Solubility

11.5 Chemical Reactions : Reactions of Haloalkanes

(I) Nucleophilic Substitution reactions (a) SN² Mechanism (b) SN¹ Mechanism © Stereochemical Aspects of Nucleophilic Substitution Reactions - Optical Activity

(I) Nucleophilic Substitution reactions (a) SN² Mechanism (b) SN¹ Mechanism © Stereochemical Aspects of Nucleophilic Substitution Reactions - Optical Activity

(I) Nucleophilic Substitution reactions (a) SN² Mechanism (b) SN¹ Mechanism © Stereochemical Aspects of Nucleophilic Substitution Reactions - Optical Activity

(ii) Elimination Reactions

(iii) Reaction with metals- Reactions of Haloarenes: (i) Nucleophilic substitution (ii) Electrophilic substitution and (iii) Reaction with metals

(iii) Reaction with metals- Reactions of Haloarenes: (i) Nucleophilic substitution (ii) Electrophilic substitution and (iii) Reaction with metals

(iii) Reaction with metals- Reactions of Haloarenes: (i) Nucleophilic substitution (ii) Electrophilic substitution and (iii) Reaction with metals

(iii) Reaction with metals- Reactions of Haloarenes: (i) Nucleophilic substitution (ii) Electrophilic substitution and (iii) Reaction with metals

11.6 Polyhalogen Compounds: Uses and Environmental Effects of Dichloromethane, Richloromethane, Triiodomethane, Tetrachloro Methane, Freons and DDT

11.6 Polyhalogen Compounds: Uses and Environmental Effects of Dichloromethane, Richloromethane, Triiodomethane, Tetrachloro Methane, Freons and DDT

11.6 Polyhalogen Compounds: Uses and Environmental Effects of Dichloromethane, Richloromethane, Triiodomethane, Tetrachloro Methane, Freons and DDT

Remaining Chapters