Docsity
Docsity

Prepare for your exams
Prepare for your exams

Study with the several resources on Docsity


Earn points to download
Earn points to download

Earn points by helping other students or get them with a premium plan


Guidelines and tips
Guidelines and tips

Organic Chem: Carbocations, Electrophiles, Nucleophiles, Alkenes & Addition Rxns., Quizzes of Organic Chemistry

Definitions and explanations of key terms related to organic chemistry, including carbocations, electrophiles, nucleophiles, alkenes, elimination products, electrophilic addition, sn1 and sn2 reactions, z and e configurations, and zaissen's and hofmann's rules. It also covers e1 and e2 mechanisms.

Typology: Quizzes

2013/2014

Uploaded on 10/31/2014

samolson09
samolson09 🇺🇸

4

(1)

17 documents

1 / 3

Toggle sidebar

Related documents


Partial preview of the text

Download Organic Chem: Carbocations, Electrophiles, Nucleophiles, Alkenes & Addition Rxns. and more Quizzes Organic Chemistry in PDF only on Docsity! TERM 1 Carbocation DEFINITION 1 Ion with a positively charged carbon atom. They are electrophilic.Tertiary: All 1st atoms are carbonsSecondary: Two first atoms are carbonsPrimary: One first atom is a carbon TERM 2 Electrophile DEFINITION 2 Wants to receive electrons, positively charged. TERM 3 Nucleophile DEFINITION 3 Wants to donate electrons, negatively charged. TERM 4 Alkene/Olefin DEFINITION 4 An unsaturated hydrocarbon containing at least one carbon- carbon double bond. CnH2n for a normal, CnH2n-2 for any cyclo-. Parent chain must contain both carbons in the double bond. The double bond gets the lowest number in numbering the parent chain The more substituted R- groups on a c=c, the more stable it is. TERM 5 Elimination Product DEFINITION 5 In this reaction, the base gains a proton (hydrogen), the halogen attached to the alpha-carbon is left, and a double bond between two carbons forms. TERM 6 Electrophilic Addition DEFINITION 6 Reaction in which a pi bond is broken to form two new sigma bonds. TERM 7 SN2 Reactions DEFINITION 7 Reactions that occur with 100% inversion (R to S, or S to R). Those with more crowded alpha carbons tend to react slower, for example an alpha carbon bonded to 3 R groups will react slower than an alpha carbon bonded to 1 R group. TERM 8 SN1 Reactions DEFINITION 8 Reactions that can occur with a mix or retention and inversion products. Products will be diastereomers. More stable organic halides react faster in these reactions. TERM 9 Z Configuration (Rank by Sequence) DEFINITION 9 Two groups of higher priority (ex. CH3) are on the same side of the c=c double bond. (Z: zusammen; together) TERM 10 E Configuration (Rank by Sequence) DEFINITION 10 Two groups of higher priority (ex. CH3) are on opposite sides of the c=c double bond. (E: entegen; opposite)
Docsity logo



Copyright © 2024 Ladybird Srl - Via Leonardo da Vinci 16, 10126, Torino, Italy - VAT 10816460017 - All rights reserved