Please answer d part (c) Draw the enol tautomers of the following molecule. Which tautomer is favored in theequilibrium and WHY?Ph(d) Which "N" is more basic and WHY?CH,(e) Identify the Michael donor and Michael acceptor that could be used to synthesize this moleculebelow:

Answer for the sub-part (d): Basicity refers to the ability of the compound to donate electrons. We…

Answered: (d) Which "N" is more basic and WHY? 2.…

Science

Chemistry

(d) Which "N" is more basic and WHY? 2. 'N' N. CH,

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter30: Orbitals And Organic Chemistry: Pericyclic Reactions

Section30.SE: Something Extra

Problem 17MP

See similar textbooks

Related questions

Q: OR A ZI

A: We have to choose which one is more basic.

Q: handwritten

A: ✓When it is pure, it is colorless.Chromium is the trace element that causes ruby's red, which ranges…

Q: Which is the stronger acid? A OR B? SEE THE PICTURE BELOW

Q: fre a) which is the most

A: According to the question, we have four free energy/reaction diagram. (a) For an exergonic…

Q: notations or notations from structures, f

A: The notations from structure of tripeptides can be drawn as

Q: B. Most Reactive I Ring B I Ring A I Ring C 3.

Q: Acoording to Organic Chemistry 3rd edition (Klein), the dienophile in the image is trans. Why is the…

A: According to nomenclature rules, the compound is named as cis and trans when the compound can show…

Q: Which is more acidic CHECH or CH2-DCH2?

A: Given that : We have to identify which of the compound is more acidic :

Q: a. Which categories/classes does this compound belong to (for example, aldehyde, ketone)? b. Draw…

A: Answer 12: a) The given molecule to class of Amides. Because it consists of amide group i.e. -CONH2.…

Q: Add the appropriate & and ô* symbols for all polar bonds in the following structures. 8. Н Н

A: The more electronegative atom has partial negative charge and the less electronegative atom has…

Q: 2) For two of the following pairs of compounds, identify the most basic atom in each compound, and…

A: Here we have to find the most basic atom and the most basic compound from the given pair of…

Q: 3) Which regresents the eno form of the following molecule?

A: Keto enol tautomerism is a type of structural isomerism. A chemical equilibrium between the keto and…

Q: How many of each atom are there on the products side?

A: Given : balance reaction of combustion of ethanol Step 1: count the no. Of atoms in both side

Q: d2 / Draw the following compounds so that they are optically active. A) Br-CH2-CH2…

A: Optically active compounds are those which are able to rotate the plane polarised light. Such…

Q: Can both compounds make hydrogen bonds? Does the second structure have a higher boilig point as it…

A: From the given two compounds, one will form hydrogen bonding and other didn't.

Q: is this molecule aromatic ，anti aromoatic，or non aromatic？？

A: Requirements for aromaticity are: Planar ring Delocalization of electrons throughout the ring (i.e.…

Q: 2. Rank the following molecules with respect to their boiling points. Explain your answer briefly. A…

A: Given molecules,

Q: A) Starting from left to right of the molecule, provide the condensed formula for the molecule below…

Q: Which has the greater delocalization energy?

A: Consider the following molecule,

Q: A C D

A: The above reactant i.e. given is form of resonating structure and from the arrows we will get a…

Q: Molecule A is more acidic compare to the molecule B? Why explain

A: In this question, we will discussed about why molecule-A is more acidic than molecule-B. molecule…

Q: Q7. One of the following two ketones is highly reactive, while the other is very stable. Which…

A: Applying concept of aromaticity and reactivity of ketone.

Q: The following compound, indicate which one you would expect to ?have the higher boling point

A: Among the various compounds, CsF will have the highest boiling point because it is the strongest…

Q: Which one is more acidic? Why?

A: According to Bronsted-Lowry concept of acids and bases Acid is a substance which can donate a…

Q: is least basic?

Q: Draw curved arrows to show how one resonance contributor leads to the next one.

A: a) Please find below the resonance contributors.

Q: Which is MORE BASIC?

Q: (a) Draw Ladenburg structures of three possible isomeric dibromobenzenes. (b) On the basis of the…

A: Albert lenderberg purpose prismane structure of benzene shown in question.

Q: NBS DMSO, H2O

A: In the reaction between alkene and NBS in water, the anti addition (because the water will attack…

Q: difference between SN1 and SN2?

A: SN1SN2The rate of reaction is unimolecular.The rate of reaction is bimolecularIt is a two-step…

Q: Explain why CH3CONH2 is a stronger acid and a weaker base than CH3CH2NH2.

A: Since the acidic strength of the compound depends on the stability of the anion formed by the…

Q: rank leaving group abililty: Cl, MeCO2, Me, NMe2, OH

A: The leaving group ability is the rate at which a reaction takes place. Leaving groups can be anions,…

Q: For molecule showed on the rightdraw the structure of 3 different conjugated basesbased on 3…

A: Resonating structures are lewis dot structures that are produced from the delocalization of electron…

Q: Curved arrows are used to illustrate the flow of electrons. Using the provided resonance structures,…

A: The arrows pushing mechanism can be shown as:

Q: Chlonnation of o berzenedicartoxylic acid Draw the molecule(s) on the canvas by choosing buttons…

Q: For each of the following pairs of molecules, which do you think should have the more acidic a…

A: A strong acid is an acid that dissociates to make protons available for reaction. Acid mainly…

Q: Which H is more acidic?

A: According to Lewis concept, acids are those substance, which are able to donate their hydrogen ions,…

Q: Which of the following resonance structures is the greatest contributor to the resonance hybrid? O:

Q: Draw a constitutional isomer of the molecule below. Try to draw it so that it does not have any…

A: The question is based on the concept of organic chemistry. We have to draw a constitution isomer.

Q: Please complete the following three graphs. Include proper axis, labels, and complete sentences…

Q: image of the pigments above, which is more polar? Why?

A: The biomolecules play an important role in the day to day life. The chlorophyll is used in…

Q: Explain why alkene A is more stable than alkene B, even though B contains more carbon atoms bonded…

A: Given compounds,

Q: most basic?

Q: Draw an exact 3-D representation of the molecule from the model.

A: Note: Since you have posted a question with multiple subparts, we will solve the first three…

Concept explainers

Photochemistry

Photochemistry is the part of chemistry that studies the various mechanisms of reactions that are triggered by the presence of light energy. It also helps to study the changes involved in a molecule that can undergo the absorption of radiation.

Question

Please answer d part

(c) Draw the enol tautomers of the following molecule. Which tautomer is favored in the
equilibrium and WHY?
Ph
(d) Which "N" is more basic and WHY?
CH,
(e) Identify the Michael donor and Michael acceptor that could be used to synthesize this molecule
below:

Expert Solution

This question has been solved!

Explore an expertly crafted, step-by-step solution for a thorough understanding of key concepts.

SEE SOLUTION Check out a sample Q&A here

Step 1

VIEW

Step 2

VIEW

Step by step

Solved in 2 steps

SEE SOLUTION Check out a sample Q&A here

Knowledge Booster

Learn more about

Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.

Similar questions

Which one is sn1 or sn2 and state the mechanism?
Draw a detailed mechanism for the FeBr3@catalyzed reaction of ethylbenzene with bromine, and show why the sigma complex (and the transition state leading to it) is lower in energy for substitution at the ortho and para positions than it is for substitution at the meta position.
Draw the ALL of the E2 organic product formed when the structure shown below undergoes dehydrohalogenation in alcoholic KOH with heat. Which of the products is formed the most?
Which compound would undergo carbocation rearrangement during an SN1 reaction? A B C D
Determine the mechanism of nucleophilic substitution of each reaction and draw the productincluding stereochemistry.
Determine if CH3CH2ONa is a suitable reagent to deprotonate the following compound. Explain why. Draw the complete reaction, including the curved arrow mechanism.
Draw a stepwise mechanism for the attached reaction that illustrateshow two substitution products are formed. Explain why 1-bromohex-2-ene reacts rapidly with a weak nucleophile (CH3OH) under SN1 reactionconditions, even though it is a 1 ° alkyl halide.
Draw the major product substitution reactions and include stereochemistry when appropriate
Although two products (A and B) are possible when naphthalene undergoes electrophilic aromatic substitution, only A is formed. Draw resonance structures for the intermediate carbocation to explain why this is observed.
Identify the reagents a-c in the following scheme:
Identify the missing reagents a-f in the following scheme:
(a) Draw a mechanism using the curved arrow-formalism for the O-4 methylation of thymine. Is thenucleophilic substitution in the first step an SN1 or SN2 reaction? Explain.