A the rate determining step is the attachment of a halogen atom to an enol intermediate.
The rate determining step is the one in which the H+ is lost from the alpha carbon to form an enol intermediate
In the mechanism of the acid-catalyzed halogenation of ketones, which of the following is NOT true?...
What is the organic product In the mechanism of the acid-catalyzed halogenation of ketones, which of the following is NOT true? A. The rate-determining step is the attachment of a halogen atom to an enol intermediate B. The first step is attachment of H^+ to the carbonyl oxygen. C. The reaction rate is independent of the halogen (X_2) concentration. D. The rate-determining step is the loss of an H^+ from an alpha-carbon to form an enol Intermediate.
Shown below is an acid-catalyzed halogenation of a ketone. What would be the first step in the mechanism? Enolate attacks the halogen Base deprotonates the alpha-carbon Nucleophile attacks carbonyl carbon Protonate the carbonyl oxygen
1. In step I the alpha bromination of ketones is acid catalyzed. a. What acid is formed as Step 1 progresses? b. Why are alpha bromination reactions acid catalyzed? 2. Substitution of bromine by t-butyl amine is the second step of the reaction today. Secondary alkyl halides can undergo substitution by Sn1 or Sn2 mechanisms. Explain (in terms of electronic interactions) why an Sn2 mechanism is favored when the halogen is alpha to a carbonyl. (Hint: Like charges on adjacent atoms are unfavorable)
chapter 18 ketones and aldehydes Which is a step in the mechanism for the acid-catalyzed hydration of propanal? A B C D
Which of the following statements is (are) true about free radical halogenation of alkanes? choose only one 1) The first of the chain-propagating steps is rate-determining. 2) The reaction proceeds by way of a flat sp2 hybridized free radical. 3) The chain-initiating step involves cleavage of a carbon-hydrogen bond to afford a carbon radical and a hydrogen atom. 4) Statements (The first of the chain-propagating steps is rate-determining) and (The reaction proceeds by way of a flat sp2 hybridized free...
What statement is TRUE about the mechanism for the reaction shown here? CH(CH) COACH CHỊ(CH3CO,CH NaOH excess heat CH,(CH2)2CO CHỊ Water attacks the carbonyl carbon to form a tetrahedral intermediate The first step of the reaction involves protonation of the ester carbonyl oxygen. One of the products formed is CH3(CH2)2CO Na. Water deprotonates the alpha carbon.
Which of the following is cyclohexane-1,4-dicarboxylic anhydride? Which of the following statements is true? A. Ester formation reactions are more violent and less easily controlled when anhydrides are uscd in place of acid chlorides. B. An acid chloride is most reactive of the common carboxylic acid derivatives because the chlorine atom causes a destabilizing inductive effect upon the carbon atom of the carbonyl group. C. Amides are more reactive than esters towards nucleophilic attack because nitrogen is less electronegative than...
oleh Secondary amines add to aldehydes and ketones to give enamines. Enamines are formed in a reversible, acid-catalyzed process that begins with nucleophilic addition of the secondary amine to the carbonyl group, followed by transfer of the proton to yield a neutral carbinolamine. Protonation of the hydroxyl group converts it into a good leaving group, however there is no hydrogen left on the nitrogen to be lost to form a neutral imine product. Instead, a proton is lost from the...
CH3 CH2 Secondary amines add to aldehydes and ketones to give enamines. Enamines are formed in a reversible, acid-catalyzed proces nucleophilic addition of the secondary amine to the carbonyl group, followed by transfer of the proton to yield a neutral carbinolanine Prosonation of the hydroxyl group converts it into a good leaving group, is no Instead, a proton is lost from the neighboring carbon to form an enamine. p, however there is no hydrogen left on the nitrogen to be...
What statement is TRUE about the mechanism for the reaction shown here? CHỊ(CH4)2COẠCH, CH,(CHỊ) CO,CH 2, CO,CH NAOH excess heat CHỊ(CH) CÓ CH, Water attacks the carbonyl carbon to form a tetrahedral intermediate. The first step of the reaction involves protonation of the ester carbonyl oxygen. One of the products formed is CH3(CH2)2CO2Na. Water deprotonates the alpha carbon.