Extra Credit An unknown compound A of molecular formula of C10H180 reacts with H2SO4 and heat...
Extra Credit An unknown compound A of molecular formula of C10H180 reacts with H2SO4 and heat to form two compounds (B and C) of molecular formula C10H16. B and C both react with H2 over Pd/C to form decalin. Ozonolysis of B forms D, and ozonolysis of C forms a diketone E of molecular formula C10H1602. Identify the structures of A, B, C and E. decalin
Extra Credit An unknown compound A of molecular formula of C10H180 reacts with H2SO4 and heat to form two compounds (B and C) of molecular formula C10H16. B and C both react with H2 over Pd/C to form decalin. Ozonolysis of B forms D, and ozonolysis of C forms a diketone E of molecular formula C10H1602. Identify the structures of A, B, C and E. O Que decalin
e) CHa .CHs На Н.с" Pt CH3 сн, 1. ВНа-THF Нас CH3 2. HO2 NaOH Br2 CH-он CH3 Extra Credit An unknown compound A of molecular formula of CjoHiO reacts with H2SO4 and heat to form two compounds (B and C) of molecular formula CioH16. B and C both react with H2 over Pd/C to form decalin. Ozonolysis of B forms D, and ozonolysis of C forms a diketone E of molecular formula CioHisO2. Identify the structures of A, B,...
Problem #1 Predict the major product(s) from the following reactions: CH3 1. 03 ? 2. DMS b) CH₃ H₂C 1. CH2CO3H 2. H3O+ CH3 CH3 HC 1. BH3-THF 2. H2O2. NaOH CH Extra Credit An unknown compound A of molecular formula of C10H180 reacts with H2SO4 and heat to form two compounds (B and C) of molecular formula C10H16. B and C both react with H2 over Pd/C to form decalin. Ozonolysis of B forms D, and ozonolysis of C...
Can someone please predict the major products and PLEASE put the
mechanism so I know how the products were achieved.
Problem #1 Predict the major product(s) from the following reactions: a) 1. O3 CH3 2. DMS CH3 b) 1. CH3CO3H ? 2. H30* CH3 cat. OsO4 - CH3 t-BuOOH d) CH3 KMnO4 cold CH3 e) CHs .CHa На Нас ? Pt CHs f) CH3 1. BH3-THF Нас ? CH3 2. H2O, NaOH g) Br2 CH3OH CHa Extra Credit An unknown...
Organic Chemistry II Question 3: Compound B has the molecular formula of C6H10 and gives (CH3)2CHCH2CH2CH3 when treated with excess H2 in the presence of Pd. B reacts with NaNH2 and CH3I to form compound C that has the molecular formula C7H12. Give the structures for B and C.
An
unknown hydrocarbon (A) with the molecular formula C9H16 reacts
with H2 and PD/C to yeild B (C9H20). Treatment of A with ozone
followed by zinc and acetic acid yielded only acetone (C) and
malonaldehyde (D). What is the structure of A and B?
7. (10pts) An nknown hydrocarbon (A) with a molecular formula CHis reacts with Ha and PdC to yield B (CH2). Treatment of A with ozone followed by zinc and acetic acid yielded only acetone (C) and...
Consider the information given below and identify the structure of the unknown compound A, with a molecular formula of C8H14. Compound A reacts with Br2/CCl4. Upon reaction of A with excess H2/Ni, 1-ethyl-2-methylcyclopentane is produced. Subjecting A to ozonolysis, the product shown below is produced as the major organic product. Draw the correct structure of compound A, and provide a brief and clear explanation relating the data provide with the structure selected.
30) 30) A compound X of molecular formula CgH12 with no triple bonds reacts with one equivalent of H2 to give a new compound having molecular formula CgH14. What can be inferred about the structure of compound X? A) Compound X has 2 rings and 1 p bond. B) Compound X has 3 p bonds. C) Compound X has 1 ring and 2 p bonds. D) Compound X has 3 rings. 31) Determine the product of the following reaction. Н....
6. An organic compound U with molecular formula C19H38 gave 2, 6, 12, 14- tetramethylpentadecane on hydrogenation. Ozonolysis of U gave propanone and a 16- carbon aldehyde V as products. Give the structures of U and V and provide the name for U. 7. An unknown hydrocarbon Q has a formula CaH12. Q Reacts with osmium tetroxide to give a diol R. When oxidized with KM O4 in an acidic medium, Q gives two products. One product is propanoic acid...