As you draw your mechanism, be sure to include all lone pair electrons and non-zero formal charges. We will use an abbreviated form of LAH, H¯, to represent the hydride ion in the mechanism. Please omit byproducts and spectator ions unless they are requested. H Use curved arrows to show how the hydride ion reacts with the ester. 00-4

As you draw your mechanism, be sure to include all lone pair electrons and non-zero formal charges. We will use an abbreviated form of LAH, H¯, to represent the hydride ion in the mechanism. Please omit byproducts and spectator ions unless they are requested. H Use curved arrows to show how the hydride ion reacts with the ester. 00-4

Chemistry for Today: General, Organic, and Biochemistry

9th Edition

ISBN:9781305960060

Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. Hansen

Publisher:Spencer L. Seager, Michael R. Slabaugh, Maren S. Hansen

Chapter14: Aldehydes And Ketones

Section: Chapter Questions

Problem 14.55E: The addition of water to aldehydes and ketones occurs rapidly, although it is not thermodynamically...

See similar textbooks

Related questions

Q: 5. The general structure of a soap molecule is shown below. The carboxylate "head" of the soap…

A: Concept: Hydrophilic: It describe something which has tends to be attracted toward water.…

Q: Draw a flowchart to show how you separate a mixture of butyric acid and hexane.

A: The butyric acid can be extracted using a NaHCO3 aqueous solution using principal of extractions.…

Q: Find the pH during the titration of 20.00 mL of 0.1000 M triethylamine, (CH3CH)3N (K, = 5.2 x 104),…

A: Since there are multiple questions, we will answer only the first one. If you require the answers to…

Q: H2N NH2

A: Oxidation of propyl benzene with KMnO4 gives benzoic acid. Reaction of benzoic acid with amine,…

Q: Draw the products resulting from addition of a Grignard reagent to an aldehyde. Use a dash or wedge…

A: Grignard reagent (RMg-X, Organo magnesium halide) is a source of carbanion which acts as a base as…

Q: Draw the product of the following reaction.

Q: Complete the reaction by adding curved arrows on the left, and product structures on the right. Be…

A: Step 1: The molecule is cyclononatetraene. You are given a base NH2- which is a strong base. Now…

Q: HO. HO. HO ОН

A: The question is based on the concept of solubility. we need to determine the solubility of gallic…

Q: What chemistry properties or structure make Salicylic acid cannot be taken orally? Is it due to the…

A: Salicylic acid is an aromatic compound with basic, -OH group and acidic -COOH group present at…

Q: How does BPA badly affect the environment?

A: BPA can affect untamed life, especially on oceanic life in both freshwater and saltwater regions,…

Question

Please draw the arrow and fix this

As you draw your mechanism, be sure to include all lone pair electrons and
non-zero formal charges. We will use an abbreviated form of LAH, H¯, to
represent the hydride ion in the mechanism. Please omit byproducts and
spectator ions unless they are requested.
H.
H
i
i
i
H
i Use curved arrows to show how the hydride ion reacts with the ester.

Expert Solution

This question has been solved!

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

This is a popular solution!

SEE SOLUTION Check out a sample Q&A here

Step 1: Writing the objective of the question

VIEW

Step 2: Predicting the mechanism

VIEW

Solution

VIEW

Trending now

This is a popular solution!

Step by step

Solved in 3 steps with 4 images

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

Predict the Intermediate and Mechanism. Predict the esterification intermediate resulting from the reaction between the starting reactants. Then, provide the complete mechanism for this reaction. You must include all appropriate arrows, intermediates, and formal charges. The ChemDraw template of this document is available on Carmen. MeO OMe དང་བ H₂SO(cat.) reflux ? OH Aromatization (Mechanism HO OH not required) Intermediate
I need help with the step 5 and 6 please
Predict the organic and inorganic products of the given reaction, and select the class to which the product belongs. Then, complete the curved-arrow mechanism. Draw the organic and inorganic products. Select Draw Rings More Erase H N H iて H The product of the reaction is Complete the mechanism of the reaction by adding any missing atoms, bonds, charges, nonbonding electron pairs, and curved arrows. Note the use of a generic base B:, O an imine. which represents another amine in solution and acts as a O an oxime. proton shuttle. a semicarbazone. O a hydrazone. 1L
The addition of water to aldehydes and ketones occurs rapidly, although it is not thermodynamically favored. What would be the product for the reaction above? Hint: Think of the self-ionization of water and the polarity of the carbonyl group.
Curved arrows are used to illustrate the flow of electrons. In this reaction, a pi bond acts as a Bronsted base. Using the provided starting structures, draw the curved electron-pushing arrows for the acid-base reaction. Be sure to account for all bond-breaking and bond-making steps. Then draw the organic product of the reaction. Include all lone pairs in the structures. Ignore inorganic byproducts and counterions. H. | H H :CIⒸ Select to Add Arrows
Draw the structure of the product of the Michael reaction between propenamide and diethyl malonate
Draw the principal organic product for the reaction when 2-bromopropane is treated with lithium in diethyl ether, followed by copper(I) iodide and then 1-bromoethane. Click and drag to start drawing a structure. X
please, complete the following reaction
Learning Complete the electron-pushing mechanism for the base-promoted hydrolysis of an ester shown in the panels. Add atoms, bonds, nonbonding electron pairs (lone pairs), charges, and curved arrows. Step 1: Complete the structure and add curved arrows. Step 2: Complete the structure and add curved arrows. ot HA
Complete the electron‑pushing mechanism for the given decarboxylation reaction. Add bonds, nonbonding electron pairs (lone pairs), and curved arrows where indicated.
Give a complete arrow-pushing mechanism for the following reactions. Show all important resonance structures of the intermediates and show exactly where each proton comes from and goes to. Indicate the Lewis acid and Lewis base (LA or LB) and whether they are also Bronsted acids and bases (BA or BB) for each intermolecular reaction. To preview image Click Here EtOH HCI (cat.) 0 LOEt OEt + H₂O
Complete the electron‑pushing mechanism for the given base‑promoted hydrolysis of an ester. Add atoms, bonds, nonbonding electron pairs (lone pairs), charges, and curved arrows where indicated.