Problem 2: Show the fragmentations for4-methyl-2-pentanone radicael carbocation and explain why thatis themost favorable path.Predict ä mass spec for the struicture, ? R CH3
Problem 2: Show the fragmentations for4-methyl-2-pentanone radicael carbocation and explain why thatis themost favorable path.Predict ä mass spec for the struicture, ? R CH3
Chemistry: Matter and Change
1st Edition
ISBN:9780078746376
Author:Dinah Zike, Laurel Dingrando, Nicholas Hainen, Cheryl Wistrom
Publisher:Dinah Zike, Laurel Dingrando, Nicholas Hainen, Cheryl Wistrom
Chapter6: The Periodic Table And Periodic Law
Section6.2: Classification Of The Elements
Problem 15SSC
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I need help with the mass spec problome
I linked a sampe example of how the queshtion needs to be answered
![Example 1: show the mostfauara ble fragrentation for 2-methylpentane
rodical carbocation.
* 86
CH3
mass 15
CH3
it
CHSCH2CH2 CH{CH3
CH3CH2 CH2¢
• cH3
methyl rodical
2° Carbocation
2- methyipentane rodical carbocetion
mass 43
CHs
블 43
+ CHCH3
2° carbocadtion
primany radicaul
This tragmentation is more favorable because a primany radical is
more stable than a methyI radical.
when answer such questians, it is best to look at tuwo possible
frogmentation paths to analyze &compare the types of radicals
carbocations that are produced, Always go with the path that offers
a more steeble carbocation andlor radičal. For this example, since
both produced 2° carbocation, the focus was on the types of radicals
is what it would (0ok like:
431 base peak
Thighe'st)
Relative
Alaundance
so
100
(m/z)
Becouse the charge on the ion is typically tl, the m/z value for a
molecular ion comesponds to He moleččular weight of the compounrd.
*Remember that the detector Keeps frack of the number of charded
particles and translates them into relative abundance. TThe
uncharged particles will not appear.](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Fac43d86a-79d6-497d-ba1c-b73403274f20%2Fcda0c2d1-81f9-4345-8122-8b8efdf01107%2F4o6uza_processed.png&w=3840&q=75)
Transcribed Image Text:Example 1: show the mostfauara ble fragrentation for 2-methylpentane
rodical carbocation.
* 86
CH3
mass 15
CH3
it
CHSCH2CH2 CH{CH3
CH3CH2 CH2¢
• cH3
methyl rodical
2° Carbocation
2- methyipentane rodical carbocetion
mass 43
CHs
블 43
+ CHCH3
2° carbocadtion
primany radicaul
This tragmentation is more favorable because a primany radical is
more stable than a methyI radical.
when answer such questians, it is best to look at tuwo possible
frogmentation paths to analyze &compare the types of radicals
carbocations that are produced, Always go with the path that offers
a more steeble carbocation andlor radičal. For this example, since
both produced 2° carbocation, the focus was on the types of radicals
is what it would (0ok like:
431 base peak
Thighe'st)
Relative
Alaundance
so
100
(m/z)
Becouse the charge on the ion is typically tl, the m/z value for a
molecular ion comesponds to He moleččular weight of the compounrd.
*Remember that the detector Keeps frack of the number of charded
particles and translates them into relative abundance. TThe
uncharged particles will not appear.
![Problem 2: Show the froagmentations for 4-methyl-2-pentanone
radlcal canoocati on and explain why that is the most
favorable path.Predicta mass spec for the stricture.
"로 100
?9? CH3](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Fac43d86a-79d6-497d-ba1c-b73403274f20%2Fcda0c2d1-81f9-4345-8122-8b8efdf01107%2Fwm0fe0d_processed.png&w=3840&q=75)
Transcribed Image Text:Problem 2: Show the froagmentations for 4-methyl-2-pentanone
radlcal canoocati on and explain why that is the most
favorable path.Predicta mass spec for the stricture.
"로 100
?9? CH3
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