(v) Ethanal reacts with HBr and the resulting product is dehydrated

Q: And which one is the major product?

A: To explain: The major product?

Q: Please help me with a drawn mechanism for the shown reaction.

A: Let's draw the mechanism: Step 1: Formation of the Enolate           O                 O(-)…

Q: TH.

A: Given images are : Increasing order of rate of nucleophilic addition = ?

Q: 19.91c1 Add curved arrow(s) to draw the first step of the mechanism. Modify the given drawing of the…

A: This is an example of Wolff Kishner reduction. The first step is the nucleophillic attack by the…

Q: Complete a mechanism for the given reaction.

A: In the above reaction, we have reactant 2 with carboxylic acid and alcohol functional group. Hence…

Q: What is the Synthesis Mechanism ? ? to form compound? reaction this OH

A: A carbonyl group comprises a carbon and an oxygen atom bonded through a double bond.The highly…

Q: why is D the best option? wouldn't A also yield the desired product?

A: Option A, i.e C6H5COOH and (CH3)3COH with H2SO4 would not give the desired tert-butyl benzoate.  The…

Q: Draw the major product of this reaction. Ignore inorganic byproducts. Assume that the water side…

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

Q: Needing the reagent, reactant, and/or the product for the following reaction. ||||| ņ LDA DIPA ?

A: LDA is a bulky base so abstract H from less hindered side . For elimination in cyclohexane both H…

Q: Explain why A is a stable compound but B is not.

A: Introduction :  We have to tell which compound is more stable.

Q: Confused on how to continue with this mechanism reaction

A:

Q: c) エ

A: c) The conversion of ethynylbenzene to 2-phenylacetaldehyde. Reagent used: Dilute H2SO4/HgSO4. This…

Q: A OH I HCI I

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

Q: explain electrophilic substitution reaction with example.

A: The replacement of any atom or group of atoms by an electrophile is termed as electrophilic…

Q: A 9.00 mL ampule of a 0.150 M solution of naphthalene in hexane is excited with a flash of light.…

A: In the world of molecular interactions, the emission of photons is a fascinating phenomenon, often…

Q: What reagents would be used in each reaction (mechanism isnt needed).  State the differences…

A: Aldol condensation reaction is condensation reaction between two aldehydes having alpha hydrogen…

Q: Provide the missing reagents. Fill in the missing reagents ? 1) 2) Br₂, FeBr ₂ 3) ? 4) ? 5) NaOH,…

A: 1)  Benzene is converted into 3-hydroxy benzoic acid .  2)  using a suitable starting material and…

Q: a) Draw all of I I 11*** the possible b) Highlight the Explain what KO+Bu LDA major makes products…

A: When an alkyl halide is treated with a strong base, the base abstracts proton from the C adjacent to…

Q: draw an efficient synthesis strategy and show all products..

A: The required step involved for this synthesis is given below-

Q: Predict the major product

A: The conjugated alkene reacts with HBr to forms allylic bromide. The regioselectivity of the reaction…

Q: draw a curved arrow mechanism for the following reaction. You may use generic acids and bases to…

A: Given reactionTo draw a curved arrow mechanism for the following reaction

Q: What steps are needed to convert A to B?

A: The given reaction is shown below.     The reaction of cycloalkene with ozone and further reaction…

Q: Which reaction will proceed? A) B) C) Both OCH3 CI Me₂CULI Me₂CuLi D) Neither

A: we have select the reaction that will occur

Q: H H : 1D -H HN-H H H- H+ Reset Drawing

A: Interpretation: We have to write reaction between ammonia and HCl using bond arrow.

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.