Compound a has the formula C10H16. on catalytic hydrogenation on Pd, it reacts with 1 molar equivalent of H2. Compound A also participates in the reaction with ozone, and then treated with Zn/H3O+ to obtain a symmetric diketon B, C10H16O2. a) How many rings does compound A contain? b) the structure of a and b c) write down the reactions that take place
We need at least 10 more requests to produce the answer.
0 / 10 have requested this problem solution
The more requests, the faster the answer.
Compound A,C10H16, reacts with 2 molar equivalent(s) of hydrogen on catalytic hydrogenation. A undergoes reaction with ozone, followed by Zn treatment, to give the above products.Propose (draw) a structure for A.
Compound A, C9H16 reacts with 1 molar equivalent(s) of hydrogen on catalytic hydrogenation. A undergoes reaction with ozone, followed by Zn treatment, to give: . Propose a structure for A.
Compound A, C12H20, reacts with 2 molar equivalent(s) of hydrogen upon catalytic hydrogenation. A undergoes reaction with ozone, followed by Zn treatment, to give: Propose a structure for A.
Compound A, C6H8, reacts with 2 molar equivalent(s) of hydrogen upon catalytic hydrogenation. A undergoes reaction with ozone, followed by Zn treatment, to give:
please explain 4. An unknown hydrocarbon has the molecular formula CH10- Upon catalytic hydrogenation over Lindlar catalyst, 1 equivalent of H2 is absorbed. On hydrogenation over a palladium catalyst, 3 equivalents of H2 are absorbed. a) How many degrees of unsaturation are present in the unknown compound? b) How many triple bonds are present? c) How many double bonds are present? d) How many rings are present? e) Draw a structure that fits the data 4. An unknown hydrocarbon has...
[Review Topics [References] Compound X has the formula C H14 X reacts with one molar equivalent of hydrogen in the presence of a palladium catalyst to form a mixture of cis- and trans-l-ethyl-3. methylcyclopentane. Treatment of X with ozone followed by zinc in aqueous acid gives a ketone and formaldehyde (CH, 0) What is the structure of X? . In cases where there is more than one answer, just draw one. -- -O0O- Compound X has the formula C,H2. X...
11. (6 pts) Hydrocarbon A has the formula C8H10. Compound A absorbs three equivalents of H2 are upon catalytic hydrogenation. When Compound A is treated with KMnO4 the following compounds form. What is the structure of A? O C-OH + HO-C-CH,CHCH2-C-OH CH3 -C-OH 3° unsat 3 the equiv
101 3. Provide the products for the following reactions below. 54K 01 OP 1) NaNH2 2) CH3BT 38 HBr (1 equiv.) ( H2. Lindlar catalyst 1) BH3. THE 2) H2O2, OH H2O, H2SO4, HgSO4 Excess Hz, Pd/C 1809 4. An unknown hydrocarbon has the molecular formula CxHjo. Upon catalytic hydrogenation over Lindlar catalyst, 1 equivalent of H2 is absorbed. On hydrogenation over a palladium catalyst, 3 equivalents of H2 are absorbed. a) How many degrees of unsaturation are present in...
Insert Delete F12 CHM210 Homework #7 Fall 2019 4. Compound A has the molecular formula C&H14. Upon catalytic hydrogenation over Pa/C it reacts with only one equivalent of hydrogen. Suggest a possible structure for Compound A. (There are MANY possible correct answers here.) Praw all of the dehydration products that are formed from the following compound.