Which compound is most susceptible to nucleophilic attack
Which compound is most susceptible to nucleophilic attack חד mais le F וד
Which carbonyl is more susceptible to nucleophilic attack, cyclohexanone or hexanal? Provide two reasons for this choice and explain each one.
addition while alkenes are most 17. Ketones are most susceptible to susceptible to addition. a. nucleophilic, electrophilic b. hydride, hydronium c. basic, acidic burd. electrophilic, nucleophilic e. reductive, oxidative 18. Addition of organolithiums or organomagnesium halides to each of the following will give a tertiary alcohol, after work-up, except for: a. carboxylic acids b. esters c. acid halides d. ketones e. none of the above solo
which compound is the most reactive for nucleophilic addition?? vs vs H most reactive which for compound Nucleophilic is the addition ?
Which acid derivative is the most reactive with respect to nucleophilic attack? CI O B O C O D
one and two 1. Aldehydes are more susceptible to nucleophilic attack than ketones. Explain. 2. Complete the following reaction scheme. РОCЬ pyridine 1. O3 NaBH 2. Me S E1OH (CH3)2CuLi SOC/2 H30*, heat 1. LIAIH NaCN Br 1. DIBALH acetone 2. Hа0 2. H30* 1. DIBALH 2. H30* HCN
Question 6 [1.5 pts] Which one of the following statements about carbons F and G is correct? O D Carbon F is more susceptible to nucleophilic attack Carbon G is more susceptible to nucleophilic attack None of the above
Which compound is expected to be the most reactive for nucleophilic acyl substitution? for en love be colo OC2H5 N(CH3)2
Which is more reactive toward nucleophilic attack, an aldehyde or a ketone? There are at least two reasons, give one
2. Which compound is expected to be the most reactive for nucleophilic acyl substitution? 3. What is the correct name of the following compound be COCH2CH2CH3 (A) propyl 4-methylhexanoate (B) propyl 5-methylhexanoate (C) propanol 4-methylhexanoic acid (D) propyl 2-methylhexanoate 4. Which ester is expected to react fastest when hydrolyzed with aqueous base? homosan hoor hoon mootto OCH3
Rank the following carbonyl-containing compounds in order of reactivity towards nucleophilic attack. Most Reactive to least reactive. 3-methylpentanoyl chloride, acetic anhydride, hexyl propanoate, N,N-diphenylethanamide, butanedial, and propanone.