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 LicenseChemistry 0871 Learning Centre
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I CH3Br CH3CH3CH2
CHCH3CH2CH2
CH3CH3CCCHCHCH3
CH2CH3
CH3CCH2CH3
OCH2CH2CH
OCH2CH3
CH3CHCHCCH2CH2CH2CH3
CH3CH2CH3
CH3ClCH2CH2CH3CH2CH2C
O OHCH2CH3
CH2CH3
12)CH3CHCHCH
CH3CH3
CH3 OH 6)CH2CHCHCH2
CH3 CH3 13)CH3CCC
CH3 CH3CH2CH3
CH3CH3CHCO
CH3 CH3 OCH3CHCHO
CH3 CH2 CH2 CH3 CH3 This work is licensed under a Creative Commons Attribution 4.0 International License 21) 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
CH3H3CH2CH2CH3
CH2CH3
CH3CH2H2CH2CH3
CH2CH3
OH BrCH2CH3
H3CCH2
CH2CH3
H3CCH2
CH2CH2CCH2CH3
OH CH3H32CH3
CH2CH3
CH3 NO2 NO2H3CCH2CH3
CH2CH3
H3C CH3 HOH3CH2CCCHCH2CH3
H3C OH3CCH2CH2CH2CH3
H3CCH2CH2CH3
CH3H3CCH2CH3
CH3 CH3H2C=CHCH2CH2CH3
H3CH=CHCH2CH3
H2C=CCH2CH3
CH3H2C=C3
CH3 H3C=3 CH3CH2CH2CH3
H3C3 OHH3CCH2CH3
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