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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 ŚDo question 4(a) (i)Describe the reaction mechanism for the hydrolysis of 2-bromo-2-methylpropane [CH3C(CH3)2Br] with aqueous hydroxide ions (OH-).
- Solving by condensation (Aldehydes and Ketones)Shown below is a carbocation intermediate in an electrophilic addition reaction of HCl with an alkene. For the conformation shown, select each hydrogen whose bond to carbon is aligned for effective hyperconjugation with the vacant p orbital on the positively charged carbon. Each adjacent carbon will have only one C-H bond so aligned. • Gray = C; white = H; red = 0; blue = N; dark green = Cl; brown =Br; light green =F; purple = I; yellow = S; orange = P. • Double click to select atoms. • You can zoom in and out using the mouse scroll wheel (or pinch to zoom on touch screens).mechanisms
- Can I have some help with this questionThe 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*4-45 In the presence of a small amount of bromine, the following light-promoted reaction has been observed. H₂C CH3 H₂C CH3 + Br₂ hv CH3 Br + H₂C. H Br (a) Write a mechanism for this reaction. Your mechanism should explain how both products are formed. (Hint: Notice which H atom has been lost in both products.) (b) Explain why only this one type of hydrogen atom has been replaced, in preference to any of the other hydrogen atoms
- The rate of hydration of 2-butene and 2-methylpropene differ by several orders of magnitude. Whcih alkene is more rapidly hydrated and why?complete the following synthesisGiven the following compounds and boiling points: Determine the IMFs Order the compounds from weakest to strongest IMFs, and Pentane (C5H12) 36°C Methane (CH4) -164°C Sodium n-butoxide (C4H9NaO) +260°C Hydrogen dioxide (H2O) 100°C