Cl H H I -H Identify the 'cartoon' drawing of the donor orbital in the nucleophilic substitution reaction of ethanoyl chloride with LiAlH4. Η Al H H CI H III H H IV H H ΑΙ H ہے A B መ II C D || III IV
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- Intramolecular H-bonding (IHB) are interactions that occur within one single molecule. IHB is also known as chelation, since it involves ring formation. Which of the following is (are) stabilized by IHB? a b c dConsider the mechanism for the given nucleophilic substitution reaction. X 2H₂0Write 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 Ś
- 7Shown 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).Write an equation for the formation of the following compounds from the appropriate alcohol
- H3C CH3 H3C NA C→XT Br Br₂ CH₂Cl₂ H3C Electrophilic addition of bromine, Br₂, to alkenes yields a 1,2-dibromoalkane. The reaction proceeds through a cyclic intermediate known as a bromonium ion. The reaction occurs in an anhydrous solvent such as CH₂Cl₂. CH3 Br In the second step of the reaction, bromide is the nucleophile and attacks at one of the carbons of the bromonium ion to yield the product. Due to steric clashes, the bromide ion always attacks the carbon from the opposite face of the bromonium ion so that a product with anti stereochemistry is formed. Draw curved arrows to show the movement of electrons in this step of the mechanism. Arrow-pushing Instructions Br CH3 H3C CH3what is the reactantDraw the structure for the nucleophilic substitution product.