The molecular formula of butane is C4H10. It is obtained from petroleum and is used commonly in LPG (Liquefied Petroleum Gas) cy
linders (a common source of cooking gas). It has two arrangements of carbon atoms: a straight chain and a branched chain. Using this information, draw the structure of the tertiary butyl radical that will form upon removal of a hydrogen atom. Draw the molecule on the canvas by choosing buttons from the Tools (for bonds).
1 answer:
Answer:
See attached picture.
Explanation:
Hello.
In this case, since butane has two common occurring structures, n-butane and isobutane, there is a way in which the tert-butyl radical can be formed upon the removal of a hydrogen from the isobutane form of butane as shown on the attached picture, wherein you can see that the radical is named by "tert" since the central carbon is bonded to three carbon atoms, that is why we classify it as tertiary. Moreover, it is a radical due to the presence of the bolded dot next to the tertiary carbon suggesting that it is very likely to bond with an other atom.
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Answer:
Explanation:
The unbalanced nuclear equation is
Let's write X as a nuclear symbol.
The main point to remember in balancing nuclear equations is that the sums of the superscripts and of the subscripts must be the same on each side of the reaction arrow.
Then
235 = 4 + A , so A = 235 - 4 = 231, and
92 = 2 + Z , so Z = 92 - 2 = 90
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Answer:
Four possible isomers (1–4) for the natural product essramycin. The structure of compound 1 was attributed to essramycin by 1H NMR, 13C NMR, HMBC, HRMS, and IR experiments.
Explanation:
Three synthetic routes were used to prepare all four compounds (Figure 2A). All three reactions utilize 2-(5-amino-4H-1,2,4-triazol-3-yl)-1-phenylethanone (5) as the precursor, whereas each uses different esters (6–8) to construct the pyrimidinone ring. Isomer 1 was prepared by reaction A, which used triazole 5 and ethyl acetoacetate (6) in acetic acid. This was the reaction used in syntheses of essramycin by the Cooper and Moody laboratories.3,4 Reaction B produced compound 2 (minor product) and compound 3 (major product), which were separated chromatographically. This reaction allowed reagent 5 to react with ethyl 3-ethoxy-2-butenoate (7) in the presence of sodium in methanol, under reflux for 24 h. Compound 4 was prepared by reaction C, which was obtained by reflux of 5 and methyl 2-butynoate (8) in n-butanol.
