Rank the following substrates in order from slowest Sy2 reaction rate to fastest. Br H3C Drag answer here fastest Br Drag answer here second slowest Br Drag answer here slowest second fastest Br Drag answer here

Q: Consider the nucleophilic substitution reaction shown here. (a) Argue whether this reaction takes…

A:

Q: b. Draw the FULL electron-pushing mechanism for the reaction depicted including ALL intermediates…

A:

Q: (Draw the product and write Fast of Slow for both) Br

A: Solution- 3-bromo pentane  will react most slowly with cyanide nucleophile (NC-) in an SN2 reaction-…

Q: Draw the curved arrow notation and products for each elementary step described by the sequence shown…

A: INTRODUCTION: E2 or bimolecular elimination is defined as a one step mechanism in which carbon…

Q: The regiochemistry in the electrophilic addition reaction shown here does not adhere to the original…

A: Markovnikov's rule  : This rule is applicable in electrophilic addition in C=C double bond.…

Q: Draw the mechanism and major product of the reaction below. Nal

A: Alkyl chloride on heating with concentrated solution of sodium iodide in acetone to form alkyl…

Q: Draw curved arrows to show electron reorganization for the reaction step below.

A: Given structure of reactant and product

Q: TH.

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

Q: Following Curved Arrows to Draw a Reaction Product Follow the curved arrows and draw the products of…

A: This reaction is an elimination reaction  In which alkyl halide is converted into an alkene with the…

Q: CO2 ОН Follow the curved arrows and draw the product of this reaction. • You do not have to consider…

A:

Q: (SYN) Which solvent-acetone or tert-butyl alcohol-would be better to use to carry out the reaction…

A: E1 reaction is a unimolecular elimination reaction, which involves the removal of an HX substituent…

Q: Br2, light

A:

Q: Below are two reactions, and one will occur faster than the other. Ts.

A: Nucleophilic substitution biomolecular reaction (SN2): The bimolecular nucleophilic substitution…

Q: How can do this reaction please O perpose mechanism

A: We have to carry out the following transformation. Also we have to give the mechanism of this…

Q: For each reaction, draw the complete, detailed mechanism and the major product. NaCl HCI ?

A: Reaction of 2-phenyloxirane with nucleophiles is being considered.

Q: at product will result from the reaction shown? (Just mention the class of compound not the…

A:

Q: a Br d Br b Br e Br Br

A: Nucleophilic substitution biomolecular reaction (SN2): The bimolecular nucleophilic substitution…

Q: Step 1 Step 2 Step 3 Step 4 i Draw H3CH2C¯, and then add the curved arrow notation showing a…

A: Nucleophilic reactions are those reactions in which a nucleophile attacks the carbon of carbonyl…

Q: For each reaction, draw the complete, detailed mechanism and the major organic product. (a) (b)…

A:

Q: Which is faster, why? # of products for each reaction? What is the mechanism of each reaction?

A: Given reaction is William son synthesis reaction in which nucleophile attacks on the alkyl…

Q: Synthetic

A:

Q: Draw the complete, detailed mechanism for the reaction shown here and predict the major products,…

A:

Q: mechanism

A: Starting material React with ethanol in acidic medium formed ester Product.

Q: For each elementary step given, determine whether the reactant or product side is favored. (a) (b)…

A:

Q: Draw the missing curved arrow notation to incidate how the carbocation in left box rearranges to the…

A:

Q: How does Carbopol work? Explain in 5 sentence

A: Carbopol is a synthetic thickening agent , which is a derivative of acrylic acid. It is used as a…

Q: 9.41 Did the following overall reaction occur by an Sn2, Sn1, E2, or E1 mechanism? How do you know?…

A: In this reaction, the Br atom is substituted by the CH3CH2O group. Hence the reaction is a…

Q: Draw the mechanism for the formation of the kinetic product of the reaction conditions shown.

A:

Q: Draw the products of the reaction and rank the reactions from fastest to slowest.

A: Nucleophilic reactions are those reactions in which a nucleophile attacks the carbon of carbonyl…

Q: Draw the reactant(s) for the following reaction.

A:

Q: Draw a detailed mechanism that shows how the starting material is converted into each of the…

A:

Q: NaNH2 `NH2 CI i) NaNH2 NH2 Br ii)

A:

Q: Draw a complete, detailed mechanism for the reaction shown here.

A:

Q: ow to know what are the best reagents to make ether efficiently? Example picture is below

A: A question based on introduction to organic chemistry that is to be accomplished.

Q: Draw the curved arrow notation and product for each of the following when they undergo an SH2 step.

A: It is given a certain reaction of the steps of a free radical mechanism and the curved arrow and the…

Q: In the electrophilic addition step shown here, where NO, adds to phenol, the electrophile can add…

A:

Q: Draw the complete, detailed mechanism for the reaction shown here and give the major product. CH3I…

A: The reaction of 4-methoxyhex-1-en-3-amine with CH3I followed SN2 mechanism results in the formation…

Q: Draw a complete, detailed mechanism for this reaction.

A: The product consists of a two phenyl groups that are joined via a carbon atoms. The structure is…

Q: Draw

A: Missing reagent should be nucleophile which attack on carbonyl carbon.

Q: Draw the missing reactant for the following reaction

A: The compound which contains ether and alcohol functional groups attached with the same carbon is…

Q: Draw the complete, detailed mechanism for the following reaction along with the major product. Cl2…

A:

Q: Draw a complete, detailed mechanism for the reaction CH3CH2OH shown here. H

A: Here the starting material is tetrahydropyran

Q: Draw the curved arrow notation and products for each elementary step described by the sequence shown…

A: Products of given reaction is

Q: 6. Explain why halogenation occurs twice in the following reaction. Ch₂ NaOH give both answer asap…

A:

Q: Use mechanism to explain the products of this reaction. Which product would be the most abundant?…

A: The mechanism of the given reaction is : Step 1 : Under UV light, Br2 undergoes homolytic cleavage…

Q: of elementary step based on the mechanistic

A: It is Tertiary Alkyl halide. So, it follows Sn1 mechanism. And it is two step mechanism.

Q: How many transition state/s is/are present in the reaction based from the energy diagram as shown…

A: Given is energy diagram.

Ionic Equilibrium

Chemical equilibrium and ionic equilibrium are two major concepts in chemistry. Ionic equilibrium deals with the equilibrium involved in an ionization process while chemical equilibrium deals with the equilibrium during a chemical change. Ionic equilibrium is established between the ions and unionized species in a system. Understanding the concept of ionic equilibrium is very important to answer the questions related to certain chemical reactions in chemistry.

Arrhenius Acid

Arrhenius acid act as a good electrolyte as it dissociates to its respective ions in the aqueous solutions. Keeping it similar to the general acid properties, Arrhenius acid also neutralizes bases and turns litmus paper into red. 

Bronsted Lowry Base In Inorganic Chemistry

Bronsted-Lowry base in inorganic chemistry is any chemical substance that can accept a proton from the other chemical substance it is reacting with.