Why is part 2 wrong, and what would be the correct organic product? :)
Why is part 2 wrong, and what would be the correct organic product? :) Be sure...
First structure is correct,
second structure is wrong and H2O is wrong
Be sure to answer all parts. Draw a stepwise mechanism for the following reaction: HBr OH CH3 CH3 Part 1 out of 2 HBr HO Br H2O HOBr CH edit structure edit structure 2 attempts left Check my work Next part
Homework marked this wrong. Not sure what I did wrong
Nat -OET ethanol This reaction involves two successive Michael reactions, and has the following steps: 1. Deprotonation forms enolate ion 1; 2. The first Michael reaction forms enolate ion 2; 3. The second Michael reaction forms enolate ion 3; 4. Protonation leads to the final product. Write the mechanism out on a sheet of paper, and then draw the structure of enolate ion 2. • You do not have to...
Provide the structure of the major organic product of the
reaction below.
Write a mechanism that explains the formation of the following
product.
Give a mechanism to account for
(2S,3R)-3-bromobutan-2-ol as a product.
H3 C CH3 (CH2CH2)2N нси We were unable to transcribe this image
Determine what is wrong with (c) Lewis structure and write the
correct structure.
Determine what is wrong with (d) Lewis structure and write the
correct structure.
We were unable to transcribe this image(b) :S-Si-S: (c) H-H O: We were unable to transcribe this image
(b) :S-Si-S:
(c) H-H O:
Add arrows to the boxes to show the mechanism of the formation
of the thermodynamic product of the reaction. All charges,
necessary lone pairs, bonds are shown, so you only have to provide
the curved arrows to convert a structure to the one in the
following box. In the last box, draw the thermodynamic product of
the reaction. Include any necessary lone pairs in your
structure.
**only the second & fourth box is wrong ** please help and
explain why....
[References] Complete the following acid-base reaction by drawing the major organic product(s). соон NaHCO, Госна • You do not have to consider stereochemistry • You do not have to explicitly draw Hatoms. • Do not include lone pairs in your answer. They will not be considered in the grading. • Include counter-ions, e.g., Na. 1. in your submission, but draw them in their own separate sketcher. • Do not draw inorganic by-products. • Draw one structure per sketcher. Add additional...
For the following unimolecular elimination reaction, draw the
intermediate (Part 1) and the product(s) (Part 2)
that would form. Include the correct stereochemistry in the
product(s).
Please explain why my above answer is
wrong.
+ CH3CH OH — We were unable to transcribe this image
For the following hydrogenation reaction, draw the correct
product and select the correct IUPAC name for the organic reactant.
(Ignore product stereochemistry in your answer.) When drawing
hydrogen atoms on a carbon atom, either include all hydrogen atoms
or none on that carbon atom, or your structure may be marked
incorrect.
For the following hydrogenation reaction, draw the correct product and select the correct IUPAC name for the organic reactant. (Ignore product stereochemistry in your answer.) When drawing hydrogen atoms...
For the following hydrogenation reaction, draw the correct
organic product and select the correct IUPAC name for the organic
reactant. When drawing hydrogen atoms on a carbon atom, either
include all hydrogen atoms or none on that carbon atom, or your
structure may be marked incorrect.
Draw the correct products, in either order, for the following
oxidative cleavage reaction.
1.Provide the major organic product of the reaction below.
2.Provide the major organic product of the reaction shown
below.
3.Provide the major organic product of the reaction shown
below.
4.Predict the necessary starting material for the reaction
below. Give the IUPAC name.
5.
Part A
Draw the carbonyl compound needed for this synthesis.
6.Predict the product formed when
CH3-CH2-C≡C:–Na+
undergoes a reaction with the compound shown below followed by an
aqueous workup..
Interactive 3D display mode
7. When 2,2-dibromo-1-phenylpropane is...