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- Write down the common (not IUPAC) names of the organic molecules that would be released if this molecule were hydrolyzed: CH₂ E CH CH,−O O || 11 O -(CH₂)7-CH=CH-CH₂-CH=CH-CH₂-CH=CH-CH₂-CH3 (CH₂)7 -CH=CH-CH₂-CH=CH-CH₂-CH=CH-CH₂-CH3 -(CH₂)16-CH3 Separate each name with a comma. You will find useful information in the ALEKS Data resource. a × Y ŚFill in the missing information—reactants, intermediatesor products—in each of the following reactions. One of these reactions does not take place as written—if no reaction occurs, state “NR”.Can you show the reaction mechanism step-by-step for C₃H₈O (l) → C3H6 (g) + H2O (l) propan-1-ol → propene + water Please show the electron movement and the way in which the bonds break. Can you please also show how many bonds there are and what type they are (eg. Sigma, Pi)? Thanks.
- USING ARROWS TO DENOTE ELECTRON FLOW- PROVIDE a detailed reaction mechanism for the reaction scheme below4. Protonation of alcohol A and subsequent loss of water, produces the intermediate B. CH3 CH; CH, CH, — с — сH, CH, CH;CH, - C- CH, CH; | OH A B (a) (i) Name alcohol A. (11) What type of species is intermediate B? (iii) Draw the structures of the two alkenes which can be formed from species B by removal of a proton. Label as C the alkene which shows geometrical isomerism. (b) The intermediate B is readily attacked by nucleophiles such as water. What is the essential feature of a nucleophile? (c) State what final colour you would see if alcohol A were warmed with acidified potassium dichromate(VI). Explain your answer. Colour Explanation . (ii) Draw two structural isomers of alcohol A which form branched chain ketones when heated with acidified potassium dichromate(VI), but which could not form alkene C on dehydration.(b) Predict the suitable solvent (H2O or CH3COCH3) to increase the reaction of bromopropane(CH3CH2CH2Br) with sodium hydroxide (NaOH). Two reactions are shown below:
- Which of the given reaction schemes would produce the molecule shown below? || ||| II and III I and II HBr ROOR || Br HBr III HBr ROOR11-15The cis and trans 2-butene stereoisomers have the following rate constant values associated with the electrophilic addition of water in an acid medium at the same temperature. what is the difference between the two values through the energy profile of each reaction. CH3 H,O productos H+ H3C k = 3.51 x 10- M's1 H3C CH3 H,0 > productos H+ k = 8.32 x 10®M's1
