Select the reagents for the following transformation. Please enter your answer as a string of capital letters with no space in between, for example: ACA A. H/Pt B. I) NANH, 2) H,0 C. IBUOK D. xs HBr E. BryH20 F. NaOEt G. BryCCl, H. EtBr I. HBr J.OYDMS K. KMNO, NAOH cold L. Na/NH M. HBr, ROOR N. 1) RCO,H, 2) H,0 O. 1) BH3. THF 2) H,O,. NaOH P. 1) Hg(OAc),, H,0 2) NaBH, Q Brg, hv R. 1) O, 2) H,O S. HLindlar's cat. T. H,O* U. HgSO,, H,SO4, H20 V. 1) R,BH 2) H,O, NAOH W. 1) xs NANH, 2) H,0 X. xs Bry/CCI Y. HCECN.
Reactive Intermediates
In chemistry, reactive intermediates are termed as short-lived, highly reactive atoms with high energy. They rapidly transform into stable particles during a chemical reaction. In specific cases, by means of matrix isolation and at low-temperature reactive intermediates can be isolated.
Hydride Shift
A hydride shift is a rearrangement of a hydrogen atom in a carbocation that occurs to make the molecule more stable. In organic chemistry, rearrangement of the carbocation is very easily seen. This rearrangement can be because of the movement of a carbocation to attain stability in the compound. Such structural reorganization movement is called a shift within molecules. After the shifting of carbocation over the different carbon then they form structural isomers of the previous existing molecule.
Vinylic Carbocation
A carbocation where the positive charge is on the alkene carbon is known as the vinyl carbocation or vinyl cation. The empirical formula for vinyl cation is C2H3+. In the vinyl carbocation, the positive charge is on the carbon atom with the double bond therefore it is sp hybridized. It is known to be a part of various reactions, for example, electrophilic addition of alkynes and solvolysis as well. It plays the role of a reactive intermediate in these reactions.
Cycloheptatrienyl Cation
It is an aromatic carbocation having a general formula, [C7 H7]+. It is also known as the aromatic tropylium ion. Its name is derived from the molecule tropine, which is a seven membered carbon atom ring. Cycloheptatriene or tropylidene was first synthesized from tropine.
Stability of Vinyl Carbocation
Carbocations are positively charged carbon atoms. It is also known as a carbonium ion.
![Select the reagents for the following transformation.
Please enter your answer as a string of capital letters with no space in between, for example:
ACA
A. H/Pt
B. I) NANH, 2) H;0
C. IBUOK
D. xs HBr
E. BryH20
F. NaOEt
G. BryCCI,
H. EtBr
I. HBr
J.OYDMS
K. KMnO, NAOH cold
L. Na/NH
M. HBr, ROOR
N. 1) RCO,H, 2) H,0"
O. 1) BH,. THF 2) H,O,. NaOH
P. 1) Hg(OAc),, H,0 2) NaBH, Q Brg, hv
R. 1) O, 2) H,O
S. HLindlar's cat.
T. H,O"
U. HgSO,, H,SO,, H20
V. 1) R,BH 2) H,O, N2OH
W. 1) xs NANH, 2) H,0
X. xs Bry/CCI
Y. HCECN.](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F622c0496-58ce-47bb-8074-5487d573c91b%2F3748073b-9d55-4b11-87fe-120034725fbd%2Fo5a9sgm_processed.jpeg&w=3840&q=75)
![](/static/compass_v2/shared-icons/check-mark.png)
Trending now
This is a popular solution!
Step by step
Solved in 2 steps with 1 images
![Blurred answer](/static/compass_v2/solution-images/blurred-answer.jpg)
![Chemistry](https://www.bartleby.com/isbn_cover_images/9781305957404/9781305957404_smallCoverImage.gif)
![Chemistry](https://www.bartleby.com/isbn_cover_images/9781259911156/9781259911156_smallCoverImage.gif)
![Principles of Instrumental Analysis](https://www.bartleby.com/isbn_cover_images/9781305577213/9781305577213_smallCoverImage.gif)
![Chemistry](https://www.bartleby.com/isbn_cover_images/9781305957404/9781305957404_smallCoverImage.gif)
![Chemistry](https://www.bartleby.com/isbn_cover_images/9781259911156/9781259911156_smallCoverImage.gif)
![Principles of Instrumental Analysis](https://www.bartleby.com/isbn_cover_images/9781305577213/9781305577213_smallCoverImage.gif)
![Organic Chemistry](https://www.bartleby.com/isbn_cover_images/9780078021558/9780078021558_smallCoverImage.gif)
![Chemistry: Principles and Reactions](https://www.bartleby.com/isbn_cover_images/9781305079373/9781305079373_smallCoverImage.gif)
![Elementary Principles of Chemical Processes, Bind…](https://www.bartleby.com/isbn_cover_images/9781118431221/9781118431221_smallCoverImage.gif)