Use electronic factors to determine which of the two intermediates is more stable. 0 A B
b) H2C=CH-CH2 1.2 Use electronic factors to determine which of the two intermediates is more stable. A B (5) 1.3 Reaction of HBr with (R)-3-methyl-3-hexanol leads to the formation of a racemic 3- bromo-3-methylhexane. a) Explain this formation with the aid of a detailed mechanism. b) Give IUPAC names of the products formed
1.2 The following reaction forms two intermediates; HBr 1.2.1 Draw the structures of the intermediates (6) 1.2.2 In not more than 2 sentences, using electronic factors, explain which intermediate is more stable (4) 1.2.3. draw and label the kinetic and thermodynamic product (6)
In each of the following ion pairs, determine which ion is
more stable. Use resonance structures to justify your
answers.
C) Etz-CH2 CH-CEN i
Q3.3 2 Points Which is more stable? O VS. 0 A B
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
Do you predict that O2 will be more or less stable than O4? What are electronic and structural differences in these molecules?
3. For the following pairs determine which molecule is more stable. Jade OR
show multistep synthesis include all reagents and stable
intermediates
COOH Cl b.
stable carbocution of Determine golloning the more pattern AIC - C&B B & A
given
Which is more stable? Position A/ Position B (circle one) COOH COOH Which is more stable? Position A/ Position B (circle one) 9. Given the results of the previous problems, if an ELECTRON DONATING group is already attached to benzene, it is more stable to add the electrophile to the _position(s). Look at positions A and B in the previous problems. a. Ortho b. Meta C. Para d. Two of the above e. None of the above 10. If...