Draw the structure for the compound C5H9Br that is consistant with H NMR. Chemical shift at 1.06, 2.0, 2.26 and 5.87.

Unknown X, C5H9Br does not react with bromine or with dilute KMnO4. Upon treatment with potassium tert-butoxide, X gives only one product, Y. Compound Y decolorizes bromine and changes KMnO4 from purple to brown. Catalytic Hydrogenation of Y gives methylcyclobutane. Ozonolysis-Reduction of Y gives dialdehyde, Z. Propose consistent structures for X,

Question: Draw the structural formula for at least one bromoalkene of molecular formula C5H9Br that shows A) No E,Z or cis-trans isomerization B) E,Z isomerization, but no cis-trans isomerization C) E,Z and cis-trans isomerization

1.Unknown X, C5H9Br, does not react with bromine or with dilute KMnO4. Upon treatment with H3O+ gives only one product, Y, C5H8. Unlike X, Y decolorizes bromine and changes KMnO4 from purple to brown. Catalyze hydrogenation of Y gives methylcyclobutane. Ozonolysis/ reduction of Y gives dialdehyde Z, C5H8O2. purpose consistent structure for X, Y ...

Question: Unknown X, C5H9Br does not react with bromine or with dilute KMnO4. Upon treatment with potassium t-butoxide, X gives only one product Y, C5H8. If X is 1-bromo-cyclopentane and Y is cyclopentene is there any aspect of X that is unknown?

Show how you would prepare monodeuteriocyclopentane (C5H9D) from bromocyclopentane (C5H9Br) using an organometallic reagent. Your solution’s ready to go! Our expert help has broken down your problem into an easy-to-learn solution you can count on.

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Draw the structures of the four bromoalkenes with the molecular formula C5H9Br that have an unbranched carbon chain, and that show chirality but not E,Z isomerism. • Use the wedge/hash bond tools to indicate stereochemistry where it exists. • If more than one structure fits the description, draw them all. • Draw one structure per sketcher.

Draw the structure of the compound that is consistent with the 1H NMR data below. (Assume that long-range coupling is not observed.) molecular formula chemical shift (ppm) relative integration multiplicity C5H9Br 1.06 3 triplet 2.00 2 multiplet 2.26 3 singlet 5.87 1 triplet

Draw line structures for at least 12 of the isomers of C5H9Br. Label cis or trans if applicable.