Draw the appropriate fishhook arrows for the following reaction,

Q: SCH3 OCH3 Br N(CH3)2 1 2 3 A) 3>1> 2>4 B) 3> 2>1>4 C) 4 > 2 > 3 >1 D) 1>3> 2 > 4

A: Order the carboxylic acid derivatives from most reactive to least reactive towards nucleophilic…

Q: Draw the following steps

A: We have to draw following given reactions in a stepwise as follows in step 2:

Q: Draw the main structure of the following reaction

A:

Q: the question is asking to: "provide a synthesis for the following reaction. if more than one step is…

A: The reaction taking place is given as,

Q: Rank the compounds in attached group in order of increasing acidity.

A: Benzoic acid: no  R and I effect.  p-methylbenzoic acid : has +R effect.  p-Chlorobenzoic acid: has…

Q: Identify the electrophile and the nucleophile in each of the following reaction steps. Then draw…

A: INTRODUCTION: Positively charged species is called as electrophile.It has an incomplete octet due to…

Q: Which of the following will undergo hydrolysis the fastest? NH

A: The reactivity of the acyl compound depends on the partial positive charge present on the carbonyl…

Q: H H CH3 CH3 -H (acid catalyst) CH3 CH3 H.

A:

Q: Draw the curved arrow formalism showing the mechanism of the following acid-base reaction and draw…

A:

Q: Draw the curved arrow mechanism for the reaction between 4-methylheptan-2-one and (CH₂O in butanol…

A: The abstraction of a hydrogen atom in the presence of a strong base is termed deprotonation. An…

Q: Which compound in each pair is the stronger acid? a. or b. or

A: (a) Cyclopentadiene is stronger acid. (b) Cyclopentadiene is stronger acid. Acidic strength is…

Q: In the presence of excess base and excess halogen, a methyl ketone is converted to a carboxylate…

A: Methyl ketone is a kind of ketone in which methyl group is attached to the carbonyl group. This…

Q: Rank the bold-faced hydrogens for the following compounds from most acidic to least acidic. Explain…

A: Lewis acids are defined as those acids which are able to lose a proton. Acidity is dependent on…

Q: Draw the appropriate reagents/ solvent

A: We’ll answer the first question since the exact one wasn’t specified. Please submit a new question…

Q: Draw the organic product of the Bronsted acid-base reaction. Include all lone pairs and charges as…

A:

Q: COULD EXPLAIN THE FOLLOWING STEPS BY ARROWS IN BASIC SOLUTION CH3 CH3 но CH2CH3 H20 CH2CH3

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Q: Which of the following hydrolysis reaction is incorrect

A: Hydrolysis is a typical type of chemical reaction in which water is used to break down chemical…

Q: Provide a plausible arrow pushing mechanism for the reaction below. CI 2 eq H20 +

A:

Q: In the following species, circle the most acidic hydrogen:

A: Acidity is defined as the tendency to release H+ in the solution. When H+ is removed then a negative…

Q: So, in this lewis acid-base reaction, do we need to draw lone pairs or not? Why or why not? Thank…

A: In the given lewis acid base reaction :  Is it necessary to represents the lone pair of electrons ?

Q: Draw a mechanism for the reaction of methylamine with formic acid. In the box to the left, draw any…

A:

Q: NaOH но. Н-О, Неat

A: When an acid and base react they form a salt and water.    Here benzoic acid react with NaOH to form…

Q: NH, H3C CH3

A:

Q: Draw the arrow-pushing mechanism for this reaction.

A: In this , an equilibrium is shown where an alcohol and enol form are in equilibrium with each other.…

Q: In the presence of excess base and excess halogen, a methyl ketone is converted to a carboxylate…

A: In halo from the reaction, A methyl ketone gets converted into carboxylate ion, and the leaving…

Q: A terminal alkyne is more acidic than an alkene and alkane because after deprotonation the lone pair…

A: Acidic strength of weak acid (organic acids) are explained by stability of its conjugate base…

Q: 2. Draw the mechanism (curved arrows) for each acid-base reaction b) d)

A: The given reactions are : Curved arrows mechanism of the given reactions are = ?

Q: a) Please draw a mechanism for the following reaction (you only have consider left to right).…

A:

Q: Which of the following would be the best base for performing the following elimination?

A: Interpretation : We have to tell which reagent is used.

Q: Please help me how to get this answer form this reaction. Can you show step by step and explain.…

A:

Q: a) Please draw a mechanism for the following reaction (you only have consider left to right).…

A:

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: NH base Z-

A:

Q: Draw the major organic product of the Bronsted acid-base reaction. Include all lone pairs and…

A: Given reaction is acid base reaction,  According to Bronsted-Lowry theory , species which donates H+…

Q: H

A: These all are derivatives of carboxylic acids. The rate of hydrolysis depends on two factors –…

Q: 1. Draw the Product (If applicable) of the Following Reactions: Br HCl

A: Detail mechanistic pathway is given below

Q: The compound below exists in two tautomeric forms. Circle the most acidic proton in the keto form…

A: Keto and enol are form of tautomerism.

Q: Which one of the following molecules can serve as a Michael acceptor?

A: Question a four compounds is given  following molecules are serve a Michael acceptar.    Michael…

Q: Draw the major organic product of the Bronsted acid-base reaction. Include all lone pairs and…

A: A Bronsted acid donates a proton and a Bronsted base accepts a proton. Hence, in a Bronsted…

Q: Which compound in the following pair is more basic?

A: The resonance structures for pyrrole are given below -  While resonance structures of piridine are…

Q: Show the mechanism for the forward acid-base reactions only

A: Acids are H+ donor and bases are H+ acceptor.  Species having negative charge has general tendency…

Q: а. Draw in any missing lone pairs b. Draw appropriate curved arrows to complete the acid-base…

A: All the three questions are answered in one chemical equation which is given on page

Q: What is the major product a or b.

A: Electron donating group increses the reactivity of benzene ring towards electrophilic substitutions.…

Q: Folow the curved arrows and draw the products of the following reaction. Include all lone pairs and…

A: Reaction 1 : strong base results in E2 elimination results double bond. Reaction 2 : bond clevage…

Q: Would this reaction go to the right, left or is it at equilibrium?

A:

Q: What is the name of product A ,Name and illustrate the effect that stabilizes Product A

A: The above mentioned question is explained below:

Q: For the following reaction step, indicate which pattern of arrow pushing it represents. A…

A:

Q: NH Ci

A: The basic Hydrolysis of Carboxylic acid derivatives give their respective Carboxylic acids with some…

Q: Provide a plausible arrow pushing mechanism for the reaction below. Note that the starting material…

A: Applying basic rule of reagents and chemical reaction.

Q: Click the "draw structure" button to launch the drawing utility. Report problem Draw the product of…

A: Carbon forms maxiumum four bonds. The oxygen atom can form maximum 2 bonds.

Designing a Synthesis

Organic synthesis is a branch of chemical synthesis that involves the planned construction of organic compounds/molecules from smaller units that possess functional groups. Friedrich Wöhler was the first scientist who designed the synthesis of an organic compound, urea from inorganic starting materials silver cyanate with ammonium chloride via a simple, one-step synthesis.