Preparation of Alkanes, Alkynes, and Alkenes Notes of Class 11th and NEET-UG 🎨

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Hydrocarbons: A Perfect Notes of Alkanes, Alkynes, and Alkenes for Class 11th and NEET-UG

Introduction:

Welcome to the exciting world of hydrocarbons, where carbon and hydrogen dance together to create a myriad of compounds. In this beginner-friendly guide, we'll explore the step-by-step process of preparing alkanes, alkynes, and alkenes, spiced up with easy-to-understand examples.

1. Alkanes: The Simple Saturations

Alkanes are like the chillers of the hydrocarbon family, keeping it simple with single carbon-carbon bonds. Imagine turning an unsaturated pal into a laid-back saturated friend - that's hydrogenation!

Example: Transforming Ethene into Ethane

C2H4+H2PtCatalystC2H6

Here, ethene (C₂H₄) kicks back with hydrogen (H₂) using a platinum (Pt) catalyst, becoming ethane (C₂H₆), a relaxed saturated alkane.

2. Alkynes: The Triple Action Heroes

Meet alkynes, the hydrocarbons with a bit of spice - carbon-carbon triple bonds. Let's transform a double-bonded duo into a triple-bonded trio through dehydrohalogenation!

Example: Turning Dibromoethane into Acetylene

CH2BrCH2Br+2NaNH2HeatHCCH+2NaBr+2NH3

Heating up 1,2-dibromoethane (CH₂Br-CH₂Br) with sodium amide (NaNH₂) transforms it into acetylene (HC≡CH), bringing that triple bond swagger.

3. Alkenes: The Double Trouble Makers

Alkenes, with their carbon-carbon double bonds, add a dash of drama. Picture removing water from an alcohol - that's dehydration leading to alkene formation!

Example: Dehydrating 2-Propanol into Propene

(CH3)2CHOHH2SO4Catalyst(CH3)2C=CH2+H2O

By using sulfuric acid (H₂SO₄) as a catalyst, 2-propanol [(CH₃)₂CHOH] loses water and transforms into propene [(CH₃)₂C=CH₂], ready to stir things up

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