Honors Chemistry Chapter 22 Problem Set 5. CH 3 CHCH 3 │ CH 3 ▬ CH ▬ CH ▬ CH ▬ CH 3 │ │ CH 3 CHCH 3 CH 2 CH 3 1. 4-ethyl-2,3-diisopropylpentane Incorrect.

Slides:



Advertisements
Similar presentations
Higher Chemistry Unit 2 Section 2 Hydrocarbons
Advertisements

Naming Hydrocarbons (nomenclature) What is a Hydrocarbon? A hydrocarbon is an organic molecule composed of carbon and hydrogen (duh). There are 3 main.
ORGANIC CHEMISTRY HYDROCARBONS Examples of Alkenes ETHENE, C 2 H 4 H C C H OR CH 2 CH 2 PROPENE CH 2 CH CH 3 TASK: Use ball & stick models or sketches.
1 Chapter 12 Unsaturated Hydrocarbons 12.3 Addition Reactions.
Prentice-Hall © 2007 General Chemistry: Chapter 16 Slide 1 of 52  Worked Examples Follow:
Isodesmic Reactions Isodesmic Reactions: chemical changes in which there is a net formal retention of the number of bonds (groups) but a change in their.
Chapter 11 Introduction to Organic Chemistry: Alkanes
1 Chapter 12 Unsaturated Hydrocarbons 12.1 Alkenes and Alkynes.
Branched Alkanes Structural Formulas Structural Isomers Table of Contents Lecture/Lab/Activity Date Pg# 22. The Periodic Table9/24/ Periodic Def.
20.7 Naming Alkenes & Alkynes Alkene formula = C n H 2n Alkyne formula = C n H 2n-2 geometric isomers cis-2-butenetrans-2-butene.
1 Chapter 12 Alkenes and Alkynes Geometric Isomers of Alkenes.
Organic chemistry.
Higher Chemistry Unit 2 Section 2 - Hydrocarbons
Organic Chemistry Topic – bonds HONC.
Basic Chemistry Copyright © 2011 Pearson Education, Inc. 1 Chapter 17 O rganic Chemistry 17.2 Alkenes, Alkynes, and Polymers.
Chemistry: An Introduction to General, Organic, and Biological Chemistry, Eleventh Edition Copyright © 2012 by Pearson Education, Inc. Chapter 11 Unsaturated.
The Hofmann Elimination. a quaternary ammonium hydroxide is the reactant and an alkene is the product is an anti elimination the leaving group is a trialkylamine.
Quiz 17 (3/26/14) 54 through 56. Provide the IUPAC name for each of the following structures: CH CH 2 =CHCH 2 CHCH 2 CH 3 4-methyl-1-hexene 55. CH.
Organic Chemistry Naming Branched Hydrocarbons 1 st Determine the longest continuous carbon chain CH 3 CH 3 CH 3 -CH 2 -CH 2 -CH-CH -CH--CH 2 –CH 3 CH-CH.
Basic Chemistry Copyright © 2011 Pearson Education, Inc. 1 Chapter 17 Organic Chemistry 17.1 Alkanes Compounds in food contain many organic compounds.
Draw the alkanes Place cards in sets at the front. 2-methylpentane 2,2-dimethylpropane octane 3-ethyl-2,5-dimethylheptane 3-ethylpentane.
5.1 Alkene Nomenclature. Alkenes Alkenes are hydrocarbons that contain a carbon-carbon double bond also called "olefins" characterized by molecular formula.
Organic Chemistry Topic – bonds HONC.
Organic Chemistry Topic 10.1 CHONCCHONC bonds.
II. Naming Hydrocarbons (nomenclature)
Organic Chemistry. Carbon Review Electron Configuration of Carbon: 1s 2 2s 2 2p 2 Valence Electrons: 4 Shape around a Carbon with all Single Bonds: Lewis.
General, Organic, and Biological Chemistry Copyright © 2010 Pearson Education, Inc.1 Chapter 17 Lipids 17.2 Fatty Acids.
Say the name of this molecule to your partner. Your partner must draw the correct molecule.
Chapter Twenty-four Organic Chemistry. Chapter Twenty-Four/ Organic Chemistry The branch of chemistry that deals with carbon compounds is organic chemistry.
Organic Chemistry Chapter 18 worgo.mp3.
Multiplication Timed Tests.
Chapter 22 Organic and Biological Molecules. Chapter 22 Organic Chemistry and Biochemistry  Organic Chemistry  The study of carbon-containing compounds.
Unsaturated Hydrocarbons Alkenes CHEMISTRY 11 MS. MCGRATH.
1. The ene suffix (ending) indicates an alkene 2. The longest chain chosen for the root name must include both carbon atoms of the double bond. 3. The.
Dr. Nesma Mamdouh Bayoumy
Naming Hydrocarbons (nomenclature)
Organic Chemistry Structural isomers Naming Branched Alkanes.
An Intro to Organic Chemistry
Naming Hydrocarbons.
Section 6 Hydrocarbons.
Organic Chemistry Organic Chemistry: The chemistry of carbon
Unit 2 Hydrocarbons.
Brief! Organic Chemistry for AP
Organic Compounds PowerPoint 5.3.
Problem ESTIMATION.
Quiz About [Your topic]
ORGANIC CHEMISTRY CHAPTER-1
Functional Groups Definition: A structural feature of a molecule, consists of a specific arrangement of atoms, responsible for certain properties of.
10.9 Preparation of Dienes 1.
Carbon Chemistry Chapter 9.
Chapter 10 Introduction to Organic Chemistry: Alkanes
Matter and Measurement
Chapter 10 Introduction to Organic Chemistry: Alkanes
Bell Work.
Structural Isomers Compounds that have the same molecular formula, but different structural formula (arrangement of atoms), are called structural isomers.
Chapter 10 Introduction to Organic Chemistry: Alkanes
Alkenes and Alkynes Learning Objectives: Keywords:
Empirical Formulas  What do all of these formulas have in common? CH C2H2C2H2 C3H3C3H3 C4H4C4H4  Empirical Formula-Reduced version of the molecular formula.
Electrophilic Addition of Hydrogen Halides to Alkenes
Aldol Condensation Reaction
Brief! Organic Chemistry for AP
Access to Science: Chemistry
Jeff Venables Northwestern High School
Naming Hydrocarbons (nomenclature)
Warmup Chapter P Review
Schedule Today (4/15): Chapter 21 Wednesday (4/17): Chapter 21
Schedule Today (4/17): Chapter 21 Friday (4/19): Chapter 21
Organic Models and Worksheet
CHEMISTRY AN INTRODUCTION TO GENERAL, ORGANIC, AND BIOLOGICAL CHEMISTRY CRS “Clicker” Questions Chapter 10 Introduction to Organic Chemistry: Alkanes.
Presentation transcript:

Honors Chemistry Chapter 22 Problem Set 5

CH 3 CHCH 3 │ CH 3 ▬ CH ▬ CH ▬ CH ▬ CH 3 │ │ CH 3 CHCH 3 CH 2 CH ethyl-2,3-diisopropylpentane Incorrect name and structure

CH 3 CHCH 3 │ CH 3 ▬ CH ▬ CH ▬ CH ▬ CH 3 │ │ CH 3 CHCH 3 CH 2 CH ,3,5-trimethyl-4-isopropylheptane Correct name and structure

a. 2,2,4-trimethylhexane b. 5-methylnonane c. 2,2,4,4-tetramethylpentane d. 3-ethyl-3-methyloctane 2.

a. 1-isopropylcyclobutane b. 1-tertbutyl-4-methylcyclopentane c. 1,3-dimethyl-2-propylcyclohexane 3.

a. 1-butene b. 4-methyl-2-hexene c. 2,5-dimethyl-3-heptene 4.

a. 2,3-dimethyl-2-butene b. 4-methyl-2-hexyne c. 2,3-dimethyl-1-pentene 5.

CH 3 CH 2 CH═CHCH 2 CH 3 6. a. b. c. CH 3 CH═ CHCH═CHCH 2 CH 3 CH 3 CHCH═CHCH 2 CH 2 CH 2 CH 3 │ CH 3

CH ≡ C ▬ CH 2 ▬ CH ▬ CH 3 │ CH 3 7. a. b. CH 3 │ CH 2 ═C ▬ C ▬CH 2 ▬CH 2 ▬CH 3 │ │ CH 3 CH 3

CH 2 CH 3 │ CH 3 CH 2 CHCH═CHCH 2 CH 2 CH 2 CH 2 CH 3 7. c.

CH 3 │ 8. CH 2 CH 3 ⁄ a.

CH 3 │ CH 3 ▬C ▬ CH 3 │ 8. b. │ CH 3 ▬C ▬ CH 3 │ CH 3

CH 2 CH 3 │ 8. \ CH 2 CH 3 c.

CH 2 CH═CHCH 3 │ 8. d.

isopropylbenzene 9.

a. 1,3-dichlorobutane b. 1,1,1-trichlorobutane c. 2,3-dichloro-2,4-dimethylhexane d. 1,2-difluoroethane 10.

a. 3-chloro-1-butene b. 1-ethyl-3-methylcyclopentene c. 3-chloro-4-propylcyclopentene d. 1,2,4-trimethylcyclohexane 11.

1-bromo-2-methylbenzene or 2-bromo-1-methylbenzene or ortho-bromotoluene or o-bromotoluene 11. e.

f. 1-bromo-2-methylcyclohexane or 2-bromo-1-methylcyclohexane g. 4-bromo-3-methylcyclohexene 11.