1-Ethyl-2-methyl-cyclopent-1-ene plus 1) O3, -78 °C; 2) (CH3)2S yields O Heptanoic acid and CO2 Pentanone and propanal Butanoic acid Pentanoic acid and propanoic acid Octan-2,6-dione

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Chapter1: Chemical Foundations
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Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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1-Ethyl-2-methyl-cyclopent-1-ene plus 1) 03, -78 °C; 2) (CH3)2S yields
Heptanoic acid and CO2
Pentanone and propanal
Butanoic acid
Pentanoic acid and propanoic acid
Octan-2,6-dione
QUESTION 13
trans-But-2-ene treated with warm, concentrated potassium permanganate yields
acetic acid
butan-2,2-dione
butan-2,3-diol
propanone and formaldehyde
ethanal
Transcribed Image Text:1-Ethyl-2-methyl-cyclopent-1-ene plus 1) 03, -78 °C; 2) (CH3)2S yields Heptanoic acid and CO2 Pentanone and propanal Butanoic acid Pentanoic acid and propanoic acid Octan-2,6-dione QUESTION 13 trans-But-2-ene treated with warm, concentrated potassium permanganate yields acetic acid butan-2,2-dione butan-2,3-diol propanone and formaldehyde ethanal
Which of the following reactions could not have created this product?
INFRARED SPECTRUM
0.8
0.4
1000
2000
Wavenumber (cm-1)
3000
NIST Chmistry WebBook (https://webbook.nist.gov/chemistry)
Oxymercuration-demercuration
O Hydrogenation
Hydration
O SN1
O SN2
Transmitance
Transcribed Image Text:Which of the following reactions could not have created this product? INFRARED SPECTRUM 0.8 0.4 1000 2000 Wavenumber (cm-1) 3000 NIST Chmistry WebBook (https://webbook.nist.gov/chemistry) Oxymercuration-demercuration O Hydrogenation Hydration O SN1 O SN2 Transmitance
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