Alkyne hydroboration - Study guides, Class notes & Summaries

Solutions for Organic Synthesis, 5e 5th Edition by Michael Smith. Retrosynthesis, Stereochemistry, And Conformations Acids And Bases and Addition Reactions Functional Group Exchange Reactions. Aliphatic and Aromatic Substitution, and Elimination Reactions Acids, Bases, And Functional Group Exchange Reactions. Acyl Addition and Acyl Substitution Functional Groups Exchange Reactions. Protecting Groups Functional Group Exchange Reactions. Oxidations Functional Group Exchange Reactions. Re...

H-X CCl4 ADD STRONG ACIDS, -hydrohalogens - Mark w H-shift + cat. (X= Cl, Br, I) SYN+ANTI H2O H2SO4 ADD WEAK ACIDS, -hydration -Mark SYN + ANI Cl2, Br2, I2 CCl4 ADD X2 (Cl, Br, I), halogenation ANTI Cl2, Br2, I2 H2O / R-OH ADD halogen and OH halohydrin ANTI 1) NCS, NBS, NIS 2) H2O / R-OH ADD halogen and OH halohydrin ANTI H-OX/ R-OX (X=Cl, Br, I) ADD halogen (X) and OH halohydrin ANTI 1) BH3 2) NaOH, H2O2 ADD OH and H hydrobo...

less the more s character a carbocation has, the _____stable it is the same as when looking at an epoxide, the orientation around the oxygen is _________ the orientation around the double bond in the reactant BrOH when added with base makes an epoxide Br2 adds 2 Brs in anti conformation lindlar catalyst produces a Z alkene from an alkyne (adds 2 Hs in syn) add more electronegative atom, add pi bond 2 ways of producing an oxidation reaction remove e...

less - the more s character a carbocation has, the _____stable it is the same as - when looking at an epoxide, the orientation around the oxygen is _________ the orientation around the double bond in the reactant BrOH - when added with base makes an epoxide Br2 - adds 2 Brs in anti conformation lindlar catalyst - produces a Z alkene from an alkyne (adds 2 Hs in syn) add more electronegative atom, add pi bond - 2 ways of producing an oxidation reaction remove e...

Chapter 3 -- Alkenes and Alkynes MULTIPLE CHOICE 1. Which of the following dienes can be classified as conjugated? A) CH3CH=C=CH2 B) CH3CH=CHCH=CH2 C) CH2=CHCH2CH=CH2 D) CH3CH=CHCH2CH2CH=CH2 E) CH2=C=CH2 ANS: B TOP: Alkenes and Alkynes: Nomenclature and Structure 2. Which of the following molecular formulas could not represent an alkene? A) C5H10 B) C7H14 C) C10H20 D) C27H56 E) C31H62 ANS: D TOP: Alkenes and Alkynes: Nomenclature and Structure 3. What...

University of Texas CH320M SN1, SN2, E1, E2, Alkene, Alkyne, mechanism map, reactions, summary sheets Hydroboration oxidation

Chapter 9 introduces alkynes. Students should already have prior knowledge about alkenes and will be pleased to know that the IUPAC naming system is similar. Students will learn how alkynes can be reduced into alkenes or alkanes. It is also important to take note of the different reagents and bases used to carry out these reactions. Students will also learn how carbon atoms can be added to or eliminated from a chain. Chapter 10 then introduces radical reactions which will be a very new concept t...

preparation of aldehydes and ketones from common reagents via oxidation or reduction

This document is a summary of the aldehydes and ketones chapter of the organic chemistry 2 course. It is digitally taken, handwritten notes. It covers information including nomenclature, synthesis and reactions with strong and weak nucleophiles. It also shows how to make hemi-acetals and acetals. Other reactions include the Wittig reaction and how to synthesize and Ylide. Notes are color coded and shortened for easy understanding and reviewing.

Introduction to E2, E1, and alkyne reactions