1. LIAIH, (3) R-C N 2. H20 NH2 1° Amine Nitrile Но н HC R (or H) 1. NaBH, or LIAIH R (or H) .C. HC (4) 2. NH,CI, H20

Q: Pair the letter under each structure with the appropriate degree of the amine from the drop-down…

A: The degree of the amine has to be given,

Q: Draw (HC(CH3)2)2

A: During drawing structure, we have to keep in mind that carbon forms four bond.

Q: 3) 2) 10) 11) 12) ic + 요요 √²+H-N= LON H ЕТ LIOH OH Socia OH Amine Protecting Group. - aff YOUNOH…

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Q: d. Ethyl propyl ether, CH3CH2OCH2CH-CH3 e. 4-hydroxy-2-butanone, CH3COCH2CH2OH f.…

A: Few questions based on Lewis structure, which are to be accomplished.

Q: NaOH(trace) a). CHO H20 HCltrace) b). H20 c). NaOH trace) H20

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Q: Q 20 Complete the following reaction: NC. NaOCH3 ELOH Ph NC Ph Ph CN CN Ph Ph NC

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Q: но H H. H. он + 3H20 -C H. H H H. H. 1. H,0' H-C- H-C -C- -C- -C H 2. H H но †N\CH»¾Ñ-Č(CH»),T+ 2n…

A: Polymerization are classified in chain polymerization, step growth polymerization. Now chain…

Q: Q2. Label all functional groups in the below antibiotic: ŅH2 H .N. CH3 .S. `CH3 HO

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Q: e basic anions?

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Q: 4. (4a) + NaHCOз - H2O + _(4b) 5. CH3COOH ± CH;CH2OCOCH3 + Hо -СОСН 6. _(6a)_ (6b)_→ + H2O

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Q: What is the molecular formula of each drug?

A: a) CHLOROQUINE drug used for antimalarial medication MOLECULAR FORMULA: C18H26ClN3 MOLAR MASS: 319:…

Q: 4. Draw in all the lone pairs on each structure. Briefly compare the size/shape of each molecule.…

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Q: Question 5 L Give the reagents. O mCPBA O 1. BH3, 2. H2O2, NaOH O KMnO4, H2O 03 1. Hg(OAc)2, H₂O 2.…

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Q: Scheme 1 Model A. Methanol: Model B. Methanol amine + red ball- no need of the H yellow red ball +…

A: No Methanol and methanol amine can't overlap each other because for overlapping all substituent must…

Q: um what is the Mechanis. 2% NaOH Me Me Me ELOH Me 94:6 P.M. McCurmy Ir Chamistry 1974, 39, 2316

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Q: Name the functional groups present in compounds 1,2 and 3 and what kind of noncovalent bonding…

A: A question based on chemical bonding, which is to be accomplished.

Q: Help me pls

A: The products are as follows:

Q: CH; Q 29. CH; C-CH,-Č-H CH, CH, The correct IUPAC name for the compound above is Oa.…

A: IUPAC is the worldwide accepted nomenclature system for chemical compounds. From the IUPAC name ist…

Q: OH HH HHHH HHHH HHE I I II IILI Н-о—с-с -С-с-с-с-с-с-С-С-с-с-с- HHH I | | L -с-с-с-—С-н H H HHH H H…

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Q: .CC14 is 44 A- Polar O B - Not polar O CH3CI is 45 A -Polar B - Not polar O Hexane readily dissolved…

A: Since, you have multiple questions. So, I will give first three questions for you. You can see the…

Q: NH2 Et3N

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Q: 1.1 equivalent LDA, -78 °C 2. CH;CH,Br

A: LDA preferentially abstracts proton form less - sterically hindered site because it is a bulky base.…

Q: Structure IV is an example of но но. он он он но- но- но- но- но- но- -H HO -H H- -он H- -OH H- OH…

A: Concept - Monosaccharides are the simplest carbohydrates since they cannot be hydrolyzed to smaller…

Q: HO- 1. Hg(OAc)2, 2. NaBH4 NaOH Br HO,

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Q: Can you help with questin 5?

A: To find: the molecule that would on steric grounds, form a stable host-guest complex with beta…

Q: 5) 6) 7) 8) 9) R SR R" mgar Meo Me '•N•" H HCI pyridine 요 R H J HO. R "P(OET)2 HOCO₂R CH3C(OET) 3…

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Q: I have no idea how to do this. Could you please explain #3 to me?

A: According to Hess law, the total enthalpy change of the reaction is the sum of all the changes. The…

Q: Is this molecule hydrophilic, amphiphilic, or hydrophobic? H,C-N-CH, CH, Q Zoom Hydrophilic B…

A: Introduction: We have to identify the molecule.

Q: 1. Lit :E 2. HCI Br2, H20 Isunepe enc toss1gwolol ert to rlose 107 (2nion S bonsdmun ed bluorde…

A: Hello. Since your question has multiple sub-parts, we will solve first three sub-parts for you. If…

Q: The Ka of methanol is 5.01 * 10-16. Which side of the following reaction is favored, reactants or…

A: There is one way to determine the whether the reactants and products are favored in a equilibrium.…

Q: Choose one of organic compounds (Eg: benzoic acid) that we always found in our daily life. State the…

A: To find : one of organic compounds (Eg: benzoic acid) that we always found in our daily life along…

Q: a) d is -bromoanil + L:OH anediamine arbons (etha ched to the ー4 nine. -NH,?

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Q: For each structure on the left, pick an identification on the right. Clear All но- -(CH2)4 -OH amino…

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Q: 1. 1. SOCI2, pyridine 2. NaOH, H20 Me 3. D2, Pd/C, EtOAc HO, Me D A B Me Me Me Me "D "D .. Me D Me D…

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Q: 4-Methylphenol, CH3C6H4OH (pKa 10.26), is only slightly soluble in water, but its sodium salt,…

A: 4-methyl phenol or para-cresol is insoluble in water because it is not enough acidic. On reaction…

Q: 1. Give the IUPAC names for the following compounds: la) CH3 (b) он CH3CHCHCH2CH3 CH2CH2CH, Ic) он…

A: Hi  Thank you for  question.  But i have been asked to solve only part 1. So please if you want more…

Q: 4. (4а) + NaHCOз — Нао + (4b)_ 5. CH;COOH t CH;CH2OCOCH3 + H20 -COCH3 6. (6а) (6b) - + H2O

A: note: as per our company guidelines, we are supposed to answer Only 1st question at a time. Still I…

Q: [H+] H20 A none of these но осн но OH но- OCH3

A: Answer: This is a three step reaction In the first step hydrogen ion will attack on the singe bonded…

Q: What type of reaction is shown below? PbSO4(aq) + 2HCl(aq) ==> PbCl2(s) + H2SO4(aq) What is…

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Q: Draw the amide formed when isopropylamine (CH₂CH(CH3)NH₂) is heated with each carboxylic acid.…

A:

Q: H3O+ /A a. H3C-OH H3O+ /A b. CH;CH-OH POC3 / pyridine C. HO. OH H2SO4 /A d.

A: a. Methanol undergo protonation to give protonated methanol which is attacked by CH3OH to give…

Q: OH OH Na2Cr207 H3O* Select to Draw

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A: A question based on properties of solution, which is to be accomplished.

Q: can function as a Léwis acid. O CH2CH2 O CN O Cr(NO3)3 O CH3NH2

A: Lewis acid which gain lone pair of electron

Q: Draw the structures of the intermediates and product of the following reaction.

A: Organic synthesis is a branch of organic chemistry which involves preparation, isolation and…

Q: For each structure on the left, pick an identification on the right. Clear All NH2 (CH)-NH2 amino…

A: The compounds given are,

Q: Place these in order of most likely to remain reactants (and not proceed to products), where 1 is…

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Q: le answer choices a 10 A в CI

A: Introduction: We have to choose which of the following has large dipole moment.

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.