Can someone please explain why the ordering is A>D>B>E>C I know why c is first because...
16.) Within each of the following sets of alkyl radicals, name each radical; identify each as either primary, secondary, or tertiary; rank in order of decreasing stability; and sketch an orbital picture of the most stable radical, showing the hyper conjugative interaction(s). (a) CH3CH2C·HCH3 and CH3CH2CH2CH2 · (b) (CH3CH2)2CHCH2 · and (CH3CH2)2C·CH3 (c) (CH3)2CHC·HCH3 , (CH3)2C·CH2CH3 and (CH3)2CHCH2CH2· (I put the lone electron after the radical carbon.) Also, my main question is in bold. The rest I know and understand....
Can someone explain how I am supposed to know which is least reactive compared to most reactive? I know that the benzene with the NO2 group on it is least reactive because it's an EWG (electron withdrawing group) so a deactivator but how do I compare the others? Thanks!!! Rank the following compounds in order of their reactivity toward electrophilic aromatic substitution NO2 CH least reactive (slowest) most reactive (fastest) b Rank the following compounds in order of their reactivity...
please help and explain why Arrange the complexes in order of decreasing stability. Rank from most stable to least stable. To rank items as equivalent, overlap them. ► View Available Hint(s) Reset Help [Cu(NE),J") (Milan) fi:0at") [fiem,)” [Peral") Most stable Least stable
Can someone please explain this one to me. I know the right answer (it is marked), but I do not understand why the first option is also not the correct answer. Any help is appreciated, thank you.
Can someone please help me with this and explain how they know stability? List the following radicals in order of increasing stability.
Can someone explain how to determine which is more stable in simple layman terms because I don't understand which is more stable just by looking. I understand how it is supposed to look in a 3d format, I understand bond angles and strains but I must not fully understand if I cant look at these two and know which is more stable. Thanks in advance! CH; and CHE CH3
So I know the answer here, but can someone explain to me how to do it and why it's D? Thanks. D Individuals IV-3 and IV-4 got married without knowing that they were related. What is the probability of their first child to have the genetic condition that runs in the family? A. 1/24 B. 1/32 C. 1/48 D. 1/72 E. A different fraction
Can someone help explain how to know when they are staggered or eclipsed? And how to draw the Newman projection. I’m a little fuzzy when it comes to the larger molecules. Also b and c please! Thank you Draw the Newman projection formula for all conformations of butane. (a) Classify them as either eclipsed or staggered conformers. entify them as either anti or gauche conformers in case of staggered conformers. (c) Rank all conformers in the increasing order of stability....
I know the answer is C, but can someone explain why it is C? Which base should be used to quantitatively convert this N,N-dimethylamide into its enolate ion?
I know the answer is C, but can someone explain why it is C? I thought the answer was A, where does the extra Oxygen come from in C? Table sugar is (+)-sucrose. Which of these products forms as the result of enzymatic or acid-catalyzed test-tube hydrolysis?