H NO2 A) H2C=CHNO2 B) CH;CH-CHNO, C) + H2C-CHNO, D) + H,C-CH2

Q: Complete the following reactions? i). NABH,/ethanol H. ii). H3O* i). LIAIH,/ether ii). H3O*

A:

Q: H3C HO.

A: The question is based on the concept of IUPAC naming of the organic compounds.   there are certain…

Q: RX .R AIX3 R R `R H2, Pd AIX3 ELOH

A: Friedel craft alkylation reaction allowed for th formation of alkyl benzenes from alkyl halides, but…

Q: Draw the structures of the following molecules. 4-bromo-5-ethoxypentanal…

A: In the above question, IUPAC name is given and it has been converted into its structure. Every…

Q: In the Acid-Base reaction described by the chemical equation below, which of the substances is…

A: Bronsted- Lowry Concept According to this concept an acid is a substance which can donate a proton…

Q: Dimethyl cyclopropanes can be prepared by the reaction of an a,ß-unsaturated carbonyl compound X…

A:

Q: Would you help me with the number 9 question? Also, can you show me the step-by-step and formula?

A:

Q: 2. Identify the overlap of hybrid orbitals present in each chemical bond indicated by the arrow…

A: “Since you have asked multiple question, we will solve the first question for you. If you want any…

Q: Draw the compound.

A: Proton-NMR spectroscopy is mainly used for the identification of type and nature of hydrogen. It is…

Q: Consider the reaction below. What functional group is present in the reactant; and, what type of…

A:

Q: Determine the structure of the product in the image below: HO Select one: HO

A: This is a chemical reaction where a proton abstraction by a base occurs to form the product.

Q: need name of structure with carbons and hydrogens labeled?

A:

Q: a) (3R,4S)-4-chloro-2,3,6-trimethylheptane b) cyclopropylcyclobutane c)…

A: The structures of given compounds would be drawn using the IUPAC nomenclature rules.

Q: 1. Fill in the missing arrows or products, as appropriate.' Hö: • H-a: a) HOH O.. b) :OH O.. :OH ÖH…

A: The curved arrow shows the movement of the electrons:

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

A: Lithium aluminium hydride, LiAlH4  is a powerful reducing agent commonly used in organic synthesis…

Q: te

A: For the nomenclature of organic compounds we follow certain rules ;  1) choose a parent chain (the…

Q: Part A a. ? 40\ NN Draw the molecule on the canvas by choosing buttons from the Tools (for bonds),…

A:

Q: 13.43 Predict the products of the following reactions. (a) 。 (b) (c) + OMe CN 우 A

A: Since you have asked question with multiple sub parts. we will solve the first three subparts for…

Q: KMNO4, NaOH H2SO4 cold H2O

A:

Q: Draw Homosalate structure and circle the parts of the structure that interacts with UV light.

A: In spectroscopy, every compound produces the peaks according the element or structure of it. The…

Q: Draw the Lewis structure of IF:O. (with minimized formal charges) and then determine the ideal…

A: The detailed solution of your question given below-. Since, we know that if a structure have…

Q: 2. Predict the product(s) of the following reaction using a step-by-step mechanism. Show all steps…

A: Given reaction is Sn2 substitution reaction.

Q: please draw the structure of the compounds named below in skeletal ('zig-zag') format, explicitly…

A: The structures in skeletal form of the following compounds has to be determined:…

Q: What would the product structure(s) be?

A: A question based on reactions of alkene. An alkene and a diene are given whose product of reaction…

Q: Complete the reaction. Include hydrogens and charges

A:

Q: In the reaction between vanillin and para-toluidine (imine formation) the product is an imine and...…

A: The reactants given are vanillin and para-toluidine. And the product given is an imine.

Q: 1. LIAIH4 (excess) 2. H3O* IZ

A: Given Product = To be determined

Q: Give the products of the reaction. excess CH;OH H* CH; CH; OCH,CH;

A:

Q: Why is the H sometimes added(labeled) on structures, and sometimes it is not?

A: Bond-line structure refers to a structure where plain lines indicate that the groups are in plane of…

Q: Classify each of the following salts as an amine salt or a quaternary ammonium salt.

A:

Q: Classify the following structures as E/Z structures

A: In given question we have asked to classify the given structures into E/Z.

Q: Draw the structures of: a. (E)-1-bromo-2-methyl-2-butene b. (Z)-3-isopropyl-2-heptene

A: The structure of the compound can be written by the IUPAC name. First of all, we draw the main…

Q: Click the "draw structure" button to launch the drawing utility. Draw the product formed from LIAIH,…

A: LiAlH4 will completely reduce the Carboxylic Acid to the Alcohol as mentioned in the step- 2 as…

Q: Which of the compounds M-P would give NO REACTION if you mixed the compound shown below with a…

A: K2Cr2O7/H2SO4 is a strong oxidising agent that oxidizes primary alcohol to acid, secondary alcohol…

Q: On the molecule below, highlight all R stereocenters in red and all S stereocenters in blue. If it…

A: A carbon atom that is bonded to four different groups is termed a chiral carbon atom. It is…

Q: 9. Magnesium in an aqueous solution of sodium hydroxide

A: The product of the given reaction is shown below:

Q: Starting from the wedge-and-dash structure below, rotate the back carbon to provide the Newman…

A: Given compound is alkane.The least stable Newman conformation is eclipsed conformation.The dihedral…

Q: Indicate whether the following balanced equations involve oxidation-reduction. If they do, identify…

A: Note : Since you have posted a question with multiple sub-parts, we will solve first three sub-parts…

Q: Classify and name the above structure

A: The IUPAC name for the molecule is given below

Q: HO ОН `ОН H₂CRO4 H2O PCC DCM MnO₂ acetone

A: -> H2CrO4/H2O is reagent used for oxidation of every alcohol. -> PCC/DCM is reagent used for…

Q: Predict the products of the following reactions.

A:

Q: ОН ACO ỌAc -ОАс

A:

Reactions of Ethers

Ethers (R-O-R’) are compounds formed by replacing hydrogen atoms of an alcohol (R-OH compound) or a phenol (C6H5OH) by an aryl/ acyl group (functional group after removing single hydrogen from an aromatic ring). In this section, reaction, preparation and behavior of ethers are discussed in the context of organic chemistry.

Epoxides

Epoxides are a special class of cyclic ethers which are an important functional group in organic chemistry and generate reactive centers due to their unusual high reactivity. Due to their high reactivity, epoxides are considered to be toxic and mutagenic.

Williamson Ether Synthesis

An organic reaction in which an organohalide and a deprotonated alcohol forms ether is known as Williamson ether synthesis. Alexander Williamson developed the Williamson ether synthesis in 1850. The formation of ether in this synthesis is an SN2 reaction.