6. You are given compounds E, F, G, and H how would you make compound J? : Hint: you only need to use two of the compounds shown below ( H. E F G H

Q: a. Here are two different carbonyl bearing molecules. With the knowledge you learned so far explain…

A: Oxygen is more electronegative, therefore, it gains partial negative charge and carbonyl carbon…

Q: HCN KCN

A:

Q: Which group in following pair is assigned the higher priority? −H, −D

A: The given pair which is higher priority can be identified as −H, −D

Q: i) CH,MgBr Cycloheptanone A (C3H160) B (C3H14) i) H20 Heat Ozonolysis HO он PUH2 C (C3H1402) E…

A:

Q: f. + CÓ + 1H2

A: Given

Q: 18) Provide names for the following two compounds. Clearly circle the name you want graded for each…

A:

Q: 1. For each pair of compounds, which has the polar n bond that will undergo nucleophillic additon…

A:

Q: 6) Which structure best fits the IR shown below? HO. H. a. b.

A: Answer:

Q: The structure of compound A is shown below. OH

A: primary carbon- carbon attached to  one carbon  secondary carbon-carbon attached to 2 carbons…

Q: Complete the reaction map by matching the answers from A-E. SO3 Brz D HNO3 3, E C FeBrz CH3 CH2 CI…

A:

Q: The molecule below contains 4 carbons. Identify the carbon that is most electrophilic. A в с

A: In this question, we want to identify most Electrophilic carbon.  How we can identify, you can see…

Q: 2. a. Rank molecules A-D (1 = lowest, 4 = highest) in order of increasing boiling %3D point. Briefly…

A: There are many functional groups in the organic chemistry such as alcohols, aldehydes, ketones,…

Q: f. g. h. i.

A:

Q: a. Rank the follow radicals from least to most stable. CH3 CH3 CH3 .F A B C D Now, explain…

A: Radical is a electron deficient species. Any electron donating group stabilize it and electron…

Q: 5. Follow the curved arrows and write the products. + BF3 a. b.

A: When two molecules interact, the molecule that has HOMO attracts the molecule with the LUMO. This…

Q: Why is the 2 and 4 positions electrophilic, but the 3 position is not electrophilic ?

A:

Q: Mostly Chapter 10, propose structures for A to F. КОН CH;CH2B В Na Br A C H20 ether ether Mg ether…

A: The solution is as follows:

Q: Consider carbonyl compounds A– E attached  below. Rank A–E in order of increasing stability.

A: To check the stability of all the above carbonyl derivatives we have to check the inertness of the…

Q: Please type your answer as (Aor B) Which molecule below is the most stable. (A= left, B= right) 2.…

A:

Q: Arrange the following according to INCREASING reactivity towards E2: 1st ( least reactive)? 2nd?…

A: In E2 elimination ,the removal of proton and leaving group occurs simultaneously.The leaving group…

Q: 1. Draw the resonance structures obtained by delocalising the lone pair on heteroatom X onto the…

A: Since you have posted multiple unrelated questions, we are entitled to answer the first only.

Q: 4. In each pair, circle the anion that is more stable. CI

A: An ion bearing a positive charge is called anion. Cations and anions are present in ionic compounds.…

Q: 34-The least stable of the following compounds is: a b d e

A: Given : We have to tell which of the following is least stable.

Q: Which hydrogen is the easiest to remove by homolytic bond cleavage? H2 H, all are equivalent O H1 O…

A:

Q: Hydrolyze the molecule below in acid (HCI). No sticks, please. ONLY cyclic product(s) can be drawn…

A: Acyclic amide gets hydrolysed while lactam remains unaffected

Q: 3. Devise a separation scheme similar to the scheme in Figure 4.2. for the following four compounds.…

A: The functional groups of a molecule are the key components and it is used to provide the notable…

Q: Rank the following compounds by relative reactivity from most-to-least reactive e., more reactive…

A:

Q: 1. Illustrate and explain how the compound below can be used to produce different alkenes.

A: In this question, we will illustrating and explaining how the given compound ( which have alkyne…

Q: Mostly Chapter 10, propose structures for A to K. КОН Na CH3CH2Br Br A C H2O ether ether Mg ether 1.…

A: We know that aq KoH will do substitution reaction with haloalkane. Na ,Mg are .metal which act like…

Q: Rank A, B, and C in order of increasing SN1 reactivity.

A:

Q: Which compound shown below has the highest balling polnt? Click on a letter A through D to answer.…

A:

Q: Mostly Chapter 10, propose structures for A to F. CH3CH,Br B КОН Na Br А C H20 ether ether Mg ether…

A:

Q: 5) Draw out the mechanism for the reaction given below, then generate a text description of the…

A: Secondary alcohol, 2,3-dimethyl-2-butanol reacts with POCl3 to give transition compound which…

Q: 2. Reactivity of Aldehydes and Ketones a. Rank the following aldehydes and ketones in order from…

A: Given: Aldehydes and ketones : A, B, C, & D. The increasing order of reactivity is as follows:

Q: 2. Rank the following anions from most to least stable. a. b. d.

A: . Stability of anion depends upon the following factor :-a Resonance stabilize the anion .b Lower…

Q: 2. Using the followin each of the following:

A: Applying concept of organic molecules and their properties.

Q: RX AIX3 'R H2. Pd AIX3 ELOH Noem een nadeel van elke reaksie. Name one disadvantage for each…

A: 1st reaction is friedal crafts alkylation. Major Disadvantage of this reaction is: The halide must…

Q: how all the α-H's in the molecules below.

A: Given compounds,

Q: Draw the following: 1. The chair structures of the most stable molecule below. (Choose the most…

A: This question belong to stereochemistry organic chemistry. We will decide the stability of 2…

Q: Mostly Chapter 10, propose structures for A to K. CH3CH2BR В КОН Na Br A C H20 ether ether Mg ether…

A:

Q: 6. In the molecule shown below, identify all (a) Chiral centers with a "C" (b) Nucleophilic sites…

A: By the concept of chiral center and nucleophilic center and electrophilic center we get the answer

Q: 6. Draw a detailed arrow pushing mechanism for the following transformations: srl NaOCH3 SN2 Br +…

A: SN2 reaction proceeds with the backside attack of the nucleophile on the alkyl halide which results…

Q: 11) which molecule below has S-configuration? A B D

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

Q: 1. Consider the acid-base equilibrium shown below on the left side. Here, the base abstracts a…

A:

Q: 2. Arrange the structures below in terms of most stable to least stable. Ans a. A B b. Y Ans

A: The stability of carbocations can be explained by Inductive effect and Hyper conjunction . The…

Q: Nitromethane is quite acidic due to the stability of the nitromethane anion shown below. List two…

A: When a proton is abstracted from nitro methane, the anion obtained is stabilized. This is the reason…

Q: Label (4 > 3 > 2, etc.) the following four groups below in decreasing priority order for R and S…

A: As R and S priority we can see with the help of atomic number

Q: Illustrate the Reaction of a Radical X• with a C=C ?

A: The free radical X·with an alkene (C=C).

Q: Compound X, C3) H5y. C31 H60 reacts with excess H/Pd to give How many double bonds and how many…

A: The reaction of H2/Pd with alkene gives the corresponding alkane where two hydrogen atom will get…

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.