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- A certain hydrocarbon had the molecular formula C18H30 and contained two triple bonds. Ozonolysis gave CH₂(CH₂)CO₂H and HO₂CCH₂CH₂CO₂H as the only products. Draw a reasonable structure for this hydrocarbon. Click and drag to start drawing a structure.3) Starting from any alkene, show how you could arrive at molecular entities containing the corresponding functional groups aldehyde, alkyne or ester.Starting with ethyne, how could you make 2-bromopentane?
- 4-pyranone will readily undergo an acid-base reaction. Identify the reaction conditions that will result in the formation of an aromatic product. Then, draw the aromatic resonance product structure. Include all lone pairs in your structure. Ignore inorganic byproducts. H3O+4. How many mono-chlorination products are possible for 3-methylpentane? Draw them out.Can this alcohol be synthesized selectively by hydroboration-oxidation of an alkene?
- What is the major organic product from the reaction of 1-pentyne with 1 mole of HBr?Reaction of 2-methyl-2-butene (above) with HBr might, in principle, lead to a mixture of two alkyl bromide addition products. Draw these two alkyl bromides.a) Give the molecular formula and draw the skeletal structure for 3-bromo-3- methylhexane. b) Name (including E/Z stereochemistry) the FIVE alkenes that can produce 3-bromo-3- methylhexane on reaction with HBr. Draw the skeletal structure of each molecule.??? c) Define the type of stereoisomerism present in 3-bromo-3-methylhexane. Name and draw the tetrahedral representation of the two stereoisomers?. d) For the base-catalysed hydrolysis of 3-bromo-3-methylhexane (i.e. reaction with the nucleophile OH-): i) ii) iii) iv) State whether the reaction is likely to proceed by an SN1 or SN2 mechanism, and explain your choice Give the likely rate law for the reaction. Explain your choice. For the reaction intermediate, draw its structure and give the VSEPR description of the geometry at the reaction centre Give the names and draw the structures of the two reaction products. Explain your conclusions
- Suppose the alkene in the drawing area below is put in strong acid solution, for example a solution of HBr. Highlight each carbon that might become protonated to form a carbocation intermediate. (The carbocation intermediate might then react with something else to form a final product.) سعدDraw the overall reaction of 2-bromo-2-methylpropane with H2O to give the alcohol product. Include all by-products that form.CH=CHNO₂ (2-nitrovinyl)benzene Electrophilic substitution on (2-nitrovinyl)benzene occurs at the meta position. Draw resonance structures to show how the ring is electron-poor at the ortho and para positions. You do not have to consider stereochemistry. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. • Separate resonance structures using the symbol from the drop-down menu. 0 78 00-F k