During the second reaction of glycolysis, the carbonyl group is moved from carbon 1 to carbon 2 forming the ketose fructose-6-phosphate. This is a necessary step in glycolysis because, this is an energetically favorable reaction that drives the first step in glycolysis forward the carbonyl in this position stabilizes the subsequent formation of the enediol intermediate O the position of the carbonyl will determine the cleavage point in the reverse aldol condensation two steps later O this allows transfer of une phosphate group from fructose to ADP to form ATP in the next step

Q: What is the aldol condensation product of two ketones in the presence of base and heat?…

A: The product of aldol addition reaction is  α,β-unsaturated aldehyde or ketone.

Q: draw an unsymmetrical ketone that has both kinetic and thermodynamic enolate. one side of the ketone…

A: The objective of the question is to draw an unsymmetrical ketone that has both kinetic and…

Q: Which statement best describes what is happening in step 6? (Remember, this is copied from the full…

A: In the given step left side one is imine. Imine is converted to examine  through tautomerisation

Q: Draw the complete mechanism for this reaction. Include the stereochemistry at the two chirality…

A: An arrow always depicts from a region of high electron density to low electron density ; that is…

Q: need help with the aldol condensation product

A: The given reaction is an example of aldol condensation.It is a base-catalyzed condensation reaction;…

Q: None

A: Step 1: The enolate ion, a crucial intermediate in the pentanal acid-catalyzed aldol process, is…

Q: Identify all resonance forms of the enolate formed, and indicate whether or not a substantial amount…

A: Keto-enol tautomerism is the existence of chemical equilibrium among the keto form and enol form of…

Q: What is/are the major product(s) of this reaction? HE H CHO heat CHO AH TCHO CHO Сно CHO CHO CHO +…

A:

Q: Use the curved arrow formalism to draw the complete mechanism for the aldol addition reaction. (It…

A: Initially one Molecule of butyraldehyde reacts with potassium Hydroxide base, where OH- ions acts as…

Q: 1. Acetaldehyde (2 carbon aldehyde) is being reacted with hydroxide in ethanol. The hydrogen alpha…

A:

Q: Complete the following base-catalyzed Self-Aldol Condensation reaction mechanism. Draw the structure…

A: Reactant is cyclohexanone. It has alpha hydrogens which in the presence of a base can be extracted…

Q: Draw the two possible products of this reaction that result from the less stable enolate and the…

A:

Q: Curved arrows are used to illustrate the flow of electrons. Follow the curved arrows and draw the…

A: Hydroboration-oxidation reaction: Alkene reacts with boron hydride followed by treatment with…

Q: QUESTION 5 Which best explains why methyl grignard will not produce an alcohol when mixed with…

A: Grignard reagent provides a carbon nucleophilic and this carbon nucleophile can give nucleophilic…

Q: What hypothesis did the Hammond Postulate help us to craft regarding the stability of carbocations…

A: according to hammond postulates. the transition state resembles to either reactant or product which…

Q: Draw the major product of this elimination. Consider regiochemistry and stereochemistry. Ignore…

A: Given that, the reaction is:

Q: Draw structure(s) of the crossed (mixed) aldol reaction product(s) between the two carbonyl…

A: When two different molecules of an aldehyde and/or ketone in a protic solvent is reacted, it…

Q: Draw the major product of this elimination. Consider regiochemistry and stereochemistry. Ignore…

A: The objective of the question is to find the major product of the given elimination reaction by…

Q: Draw the mechanism of the following alkylation reaction that occurs via an enolate intermediate. о…

A:

Q: Is true about halohydrins, example bromohydrin the intermediate in a. the reaction mechanism is a…

A: Halohydrins are the organic molecules:

Q: Draw the transition state of this process. 애 + HOW I HO IIIIH +OI

A: A nucleophilic substitution reaction is a substitution reaction where a nucleophile replaces another…

Q: Notice in Problem 25.63 that the hydroperoxide forms at the C atom that is α to the O atom and not…

A: A free radical chain reaction involves free radicals in a cyclic sequence of steps, called…

Q: The trityl cation intermediate is a highly stable species due to the resonance stabilization…

A: Trityl cation also known as triphenylmethyl cation is very stable because the positive charge on…

Q: In witting synthesis experiment what compounds describes the oxaphosphetane intermediate? Draw

A: The reaction given is witting synthesis.

Q: Draw the major product of the aldol addition reaction between two of these aldehydes with the…

A: We have been asked to draw the major product of aldol addition of given two aldehydes.Aldehydes are…

Q: Draw the most stable resonance form for the intermediate in the following electrophilic substitution…

A: This is an electrophilic aromatic substitution reaction.

Q: Terminal alkynes have a relatively acidic proton. This proton can easily be deprotonated converting…

A: Terminal alkynes are much more acidic than most other hydrocarbons. Elimination reaction required…

Q: What is the product and draw me the mechanism OH + H+

A: In this reaction a Tertiary carbocation is formed which is being attacked by the Phenol.

Q: HCI cold

A:

Q: Draw the enolate anion and the carbonyl that would be needed to make this product through an aldol…

A: Well, We have to look very carefully the alpha-beta unsaturated carbonyl compound. we will cleave…

Q: Draw the mechanism for the last step in the Kiliani-Fischer synthesis.

A: The last step for the kiliani-Fischer synthesis has to be given.

Q: Show the steps of the following

A:

Organometallic Compounds

These are the compounds containing at least one carbon-metal bond in their molecule. It consists of metal and organic parts. These metals may be lithium, sodium, magnesium, zinc, and lead whereas the organic part can be the alkyl, aryl, alkenyl, or alkynyl group.