A compound with molecular formula C9H18 exhibits a 1H NMR spectrum with only one signal and a 13C NMR spectrum with two signals. Draw the structure of this compound. There’s just one step to solve this.

An alkene having the molecular formula C9H18 is treated sequentially with ozone (O3) and zinc/acetic acid to give the product/s shown. Draw a structural formula for the alkene. - You do not have to consider stereochemistry. - You do not have to explicitly draw H atoms. - In cases where there is more than one answer, just draw one.

Question: Compound A (C9H12) absorbed 3 equivalents of H2 on catalytic reduction over a palladium catalyst to give B (C9H18). On ozonolysis, compound A gave, among other things, a ketone that was identified as cyclohexanone. On treatment with NaNH2 in NH3, followed by addition of iodomethane, compound A gave a new hydrocarbon, C (C10H14).

An alkene with a molecular formula of C9H18 was subjected to ozonolysis, affording the two products shown below. 1) 03 + alkene C,H18 2) Mens I i) Give the IUPAC names for each of the two products. ii) Draw the structure of the alkene reactant.

Hi could you help me with this problem please " A compound with the molecular ormula C9H18 exhibits a H1 NMR spectrum with only ONE signal, and a C13 NMR spectrum with only TWO signals. Write the correct structure and the reason why that is the structure. Explain any thought processes involved in determining the correct structure " Hint: I answered

Compound A, C9H12, absorbs 3 equivalents of H2 over a palladium catalyst to give B, C9H18. On reaction with KMnO4, compound A gives, among other things, a ketone that was identified as cyclohexanone. On treatment with NaNH2 in NH3, followed by addition of iodomethane, compound A gives a new hydrocarbon C, C10H14.

What is the molecular formula of a cyclic alkane with 9 carbon atoms? a. C9H20. b. C9H16. c. C9H22. d. C9H18 . e. C9H9

3. Hydrocarbon A has the formula C9H12 and absorbs 3 equivalents of hydrogen to yield compound B(C9H18),when hydrogenated over a Pd/C catalyst. On treatment of A with aqueous sulfuric acid in the presence of mercury (II), two isomeric ketones, C and D, are produced.

Question: Compounds Y and Z both have the formula C9H18 Both Y and Z react with one molar equivalent of hydrogen in the presence of a palladium catalyst to form 2-methyloctane The heat of hydrogenation of Y is less than that of Z. Y and Z each undergo hydroboration/oxidation to give a primary alcohol (OH attached to a primary carbon What is the structure of Y? .

to yield B, C9H18, when hydrogenated over a Pd/C catalyst. On treatment. of A with aqueous H2SO4 in the presence of mercury(II), two isomeric. ketones, C and D, are produced. Oxidation of A with KMnO4. gives a mixture of acetic acid (CH3CO2H) and the tricarboxylic acid E. Propose structures for compounds A-D, and write the reactions.