Methyl nitrate, CH 2 NO 2 , is used as a rocket propellant. The skeletal structure of the molecule is CH 2 ONO 2 . The N and three O atoms all lie in the same plane, but the CH 2 group is not in the same plane as the NO 2 group. The bond angle C−O−N is 105 o , and the bond angle O−N−O is 125 o . One nitrogen-to-oxygen bond length is 136 pm, and the other two are 126 pm. Draw a sketch of the molecule showing its geometric shape. Label all the bonds in the molecule as or r, and indicate the probable orbital overlaps involved. Explain why all three nitrogen-to-oxygen bond lengths are not the same.
Methyl nitrate, CH 2 NO 2 , is used as a rocket propellant. The skeletal structure of the molecule is CH 2 ONO 2 . The N and three O atoms all lie in the same plane, but the CH 2 group is not in the same plane as the NO 2 group. The bond angle C−O−N is 105 o , and the bond angle O−N−O is 125 o . One nitrogen-to-oxygen bond length is 136 pm, and the other two are 126 pm. Draw a sketch of the molecule showing its geometric shape. Label all the bonds in the molecule as or r, and indicate the probable orbital overlaps involved. Explain why all three nitrogen-to-oxygen bond lengths are not the same.
Methyl nitrate,
CH
2
NO
2
, is used as a rocket propellant. The skeletal structure of the molecule is
CH
2
ONO
2
. The N and three O atoms all lie in the same plane, but the
CH
2
group is not in the same plane as the
NO
2
group. The bond angle C−O−N is 105o, and the bond angle O−N−O is 125o. One nitrogen-to-oxygen bond length is 136 pm, and the other two are 126 pm.
Draw a sketch of the molecule showing its geometric shape.
Label all the bonds in the molecule as or r, and indicate the probable orbital overlaps involved.
Explain why all three nitrogen-to-oxygen bond lengths are not the same.
#1. Retro-Electrochemical Reaction: A ring has been made, but the light is causing the molecule to un-
cyclize. Undo the ring into all possible molecules. (2pts, no partial credit)
hv
Don't used Ai solution
I have a question about this problem involving mechanisms and drawing curved arrows for acids and bases. I know we need to identify the nucleophile and electrophile, but are there different types of reactions? For instance, what about Grignard reagents and other types that I might not be familiar with? Can you help me with this? I want to identify the names of the mechanisms for problems 1-14, such as Gilman reagents and others. Are they all the same? Also, could you rewrite it so I can better understand? The handwriting is pretty cluttered. Additionally, I need to label the nucleophile and electrophile, but my main concern is whether those reactions differ, like the "Brønsted-Lowry acid-base mechanism, Lewis acid-base mechanism, acid-catalyzed mechanisms, acid-catalyzed reactions, base-catalyzed reactions, nucleophilic substitution mechanisms (SN1 and SN2), elimination reactions (E1 and E2), organometallic mechanisms, and so forth."
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Author:Steven D. Gammon, Ebbing, Darrell Ebbing, Steven D., Darrell; Gammon, Darrell Ebbing; Steven D. Gammon, Darrell D.; Gammon, Ebbing; Steven D. Gammon; Darrell
Author:Steven D. Gammon, Ebbing, Darrell Ebbing, Steven D., Darrell; Gammon, Darrell Ebbing; Steven D. Gammon, Darrell D.; Gammon, Ebbing; Steven D. Gammon; Darrell