[PDF] Naming Organic Compounds Practice





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Naming Alkenes

Naming Alkenes. Suffix: -ene. Many of the same rules for alkanes apply to alkenes. 1. Name the parent hydrocarbon by locating the longest carbon chain that 



Chapter 8 - Alkenes Alkynes and Aromatic Compounds

Answers. 1. Alkenes have double bonds; alkynes have triple bonds. The cis-trans naming system can be used to distinguish simple isomers where each.



ORGANIC CHEMISTRY I – PRACTICE EXERCISE Alkene reactions

This illustrates the principle of . 35) Which of the following is the best reaction sequence to accomplish a Markovnikov addition of water to an alkene with 



Naming Alkenes And Alkynes Quiz With Answers (PDF) - m.central

Chemistry Bruce Averill 2007 Emphasises on contemporary applications and an intuitive problem-solving approach that helps students discover the exciting 



Practice Set Answer Keys Organic Chemistry I Table of Contents

Test 3 PS3: Test 3 Alkene Reactions Practice. 43. Test 3 PS4: Test 3 Extra Synthesis Practice (6 pages). 45. Test 4. Test 4 PS1: Test 4 HBr Addn to Dienes; 



Naming Organic Compounds Practice

A. Identify the class of the following compounds. For any alkanes alkenes



Chapter 2 Unsaturated Hydrocarbons

Learn to recognize the alkene alkyne



Practice Tests Answer Keys Organic Chemistry I

Alkane Acyclic: CnH2n+2. Alkane Cyclic: CnH2n. Alkene: CnH2n (not expected to remember but evident if you count). Counting H's can always double-check on this!



1 Chapter 6. Alkenes: Structure and Stability Degrees of

Naming Alkenes. Suffix: -ene. Many of the same rules for alkanes apply to alkenes Indicate the double bond by the number of the first alkene carbon.



PRACTICE – ORGANIC NOMENCLATURE

Directions: Write your answers to the following questions in the space provided. Use Would an alkene be considered a saturated or unsaturated.

Authored by Emily Simpson

This work is licensed under a Creative Commons Attribution 4.0 International License

Chemistry 0871 Learning Centre

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I CH3Br CH3

CH3CH2

CHCH3CH2CH2

CH3

CH3CCCHCHCH3

CH2CH3

CH3CCH2CH3

O

CH2CH2CH

O

CH2CH3

CH3CHCHCCH2CH2CH2CH3

CH3CH2CH3

CH3Cl

CH2CH2CH3CH2CH2C

O OH

CH2CH3

CH2CH3

12)

CH3CHCHCH

CH3CH3

CH3 OH 6)

CH2CHCHCH2

CH3 CH3 13)

CH3CCC

CH3 CH3

CH2CH3

CH3

CH3CHCO

CH3 CH3 O

CH3CHCHO

CH3 CH2 CH2 CH3 CH3 This work is licensed under a Creative Commons Attribution 4.0 International License 2

1) 1-pentene 7) 4-methylhexanoic acid

2) 2-methyl-3-heptyne 8) 2,3-dichloro-4-ethyl-2-hexene

3) 3-ethyl-4,5-dimethylpentane 9) 2,4-dinitrotoluene

4) 2-ethyl-1-pentanol 10) 3-ethyl-2,3-dimethyl-2-pentanol

5) m-bromophenol 11) 5-chloro-4-methyl-3-heptanone

6) 3,3,6,6-tetraethyl-4-octyne 12) 3-phenyl-1-propyne

This work is licensed under a Creative Commons Attribution 4.0 International License 3 (7) (8) (9) (10) (11) (12)

H22CH2CH3

CH3

H3CH2CH2CH3

CH2CH3

CH3

CH2H2CH2CH3

CH2CH3

OH Br

CH2CH3

H3CCH2

CH2CH3

H3CCH2

CH2CH2CCH2CH3

OH CH3

H32CH3

CH2CH3

CH3 NO2 NO2

H3CCH2CH3

CH2CH3

H3C CH3 HO

H3CH2CCCHCH2CH3

H3C O

H3CCH2CH2CH2CH3

H3CCH2CH2CH3

CH3

H3CCH2CH3

CH3 CH3

H2C=CHCH2CH2CH3

H3CH=CHCH2CH3

H2C=CCH2CH3

CH3

H2C=C3

CH3 H3C=3 CH3

CH2CH2CH3

H3C3 OH

H3CCH2CH3

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