a. BRCH,CH,C=CCH3 c. CH3OCH,C=CCH2CH3 b. CH3CH,CHC=CCH,CHCH3 d. CH3CH,CHC=CH Br ČI CH,CH,CH3

Q: CH3 За. ВНз. ТHF Et20, EtOH B2 B1 зь. NaOH, H202 "CHз 2. Н, саt. (PҺ3P);RhCI toluene A) (a) and (b)…

A: Birch reduction is the reduction of arenes to cyclo Hexa dienes, in the presence of sodium in liquid…

Q: What is the major product of each of the following reactions?

A:

Q: a) -СCH-CH-OH,-Br,-H, -CH-CHз b) -СООН, СООCH3,-CH-ОН,-ОН с) -СH-NHCH3,-CH-NHz-NHz,-CN

A: Answer:- This question is solved by using the simple concept of determination of priority order…

Q: H2N-CHC-OH CH2 H2N-CHC-OH CHOH CH3 H2N-CHC-OH CH2 HN- H2N-CHC-OH CH2 OH

A: Amino acids:- These are basically the building blocks of protein. They contain an acid(COOH)…

Q: What orbitals are used to form the carbon–carbon s bond between the highlighted carbons?

A: To find the orbitals used to make bond we need to find the hybridisation of those 2 Carbons. And the…

Q: CH;-CH,-CH, CH,-CH3 1. CH3-CH-CH,- сH - CH, CH3 CH3 CH3 2. CH,- с - сH,-CH - CH-CH, CH3

A: Write the IUPAC NAME of the given structure-

Q: Rank the water solubility of the following compounds:

A: Given compounds,

Q: Draw the products in each reaction.

A: NOTE: Since, we only answer upto three sub-parts, we'll answer the first 3. Please resubmit the…

Q: HC=CCH,CH, CH,CH=CHCH, CH3CH2CH2CH3 С. d. HCI, H2O, H2S e. CH3CH2CH3, CICH2CH2OH, CH3CH2OH

A:

Q: 8. * CH3 CH3 CH3 CH30C, CH2CH NaOCH3 HC CH2CH3 Br Sy2 CH2CH3 VWX XwV O vWX O xwv

A: SN2 reaction:- It stands for substitution nucleophilic bimolecular. It is a bimolecular reaction…

Q: 4. H3C CH3 CH CH3-CH2-CH2-ČH-CH2-CH2-CH2-CH3 5. CH2-CH3 H3C CH CH3-CH2-CH2-CH2-CH-CH2-CH2-…

A: Rules for naming the organic compound is as follows;              Select the longest continuous…

Q: What is each compound’s systematic name?

A: Since we only answer up to 3 sub-parts, we’ll answer the first 3. Please resubmit the question and…

Q: Give the IUPAC name for each thiol.

A: IUPAC names : (a) Pentan-3-thiol   (b) Cyclohexanethiol   (c) 5-ethylheptan-1-thiol

Q: a. H3C-CH2-NH-C-H IUPAC H3C-CH2-NH-ĉ-H Common H3C-CH-CH2-CH2-CH2-C-0-CH3 b. Br IUPAC…

A: (a)  IUPAC name : N-Ethylmethanamide Common name : N-Ethyl formamide     (b)  IUPAC name :…

Q: Draw curved arrows to show the movement of the electrons that result in formation of the given…

A: Nucleophiles are the electron rich species and it can share at least a pair of electron.…

Q: Which of the following compounds can exist as cis–trans isomers?

A: The alkenes which have same groups on the same side cannot exist as cis-trans isomers.

Q: a O₂N. HO C e O₂N SO3/H₂SO4 CHO CH3 Br₂/A COCH2CH3 Zn/ (Hg) / HC1

A: a)      The 2- nitrophenol  is a process of heating  with fuming sulphuric acid (H2SO4 +SO3) to…

Q: (a) (b) CH2CH2CHO (c) CH3CH2CCHCH, CHyČCH;CH2CH;ÖCH,CH3

A: Since we only answer up to 3 sub-parts, we'll answer the first 3. Please resubmit the question and…

Q: What is each compound’s systematic name?

A:

Q: I CH3-CH2 4.CH3-CH-CH-CH2-CH-CH2-CH2-CH2-CH2-CH3 I CH3-CH2 I CH3-CH2 I CH3 5.…

A: -> For IUPAC naming following steps are required - First of all identify the longest carbon…

Q: Which of the following compounds has an asymmetric center?

A: Asymmetric centre is a molecule having a special arrangement of ligands which is not superiposable…

Q: A H. OH В C CH,CH3 D E NH CH,CH3 CH2CH3

A: The explanation of the organic reaction is given below

Q: What stereoisomers would you expect to obtain from each of the following reactions?

A:

Q: а. CH3 HCI/ZnCl2 . CH3 OH b. HCI/ZnCl2 CH3(CH2),–CHOH C. н он CH;-C-CH–CH; ċ–CH–CH, HC/ZnCl2 ČH,

A: Alcohols undergo substitution reaction with Lucas reagent. Primary alcohols follow SN2 mechanism and…

Q: CHO CHO a. (CH3),CC(CH3)2CH,CHO b. С. С

A: Naming of a compound is done according to rules given by iupac

Q: (g) NH + CH3(CH2)6CH,CI ethanol (h) -CH2CI + NH3 ethanol

A:

Q: Name the following:

A: Since the question has multiple sub-parts, we are entitled to answer only the first 3 parts.

Q: Rank the following conformations in order of increasing energy.

A: The structure A and D both are staggered conformation as it has the dihedral angle as sixty.  The…

Q: CH;CH2CH2CH,CI CH3 CH3CH2CH,ČOCH,CHCH3 CH;CH,CH,CH,CH2CN(CH3)2

A: For naming first of all select longest hydrocarbon chain containing functional group . Then number…

Q: (a) Br CH3CHCH₂CH₂CH₂C(CH3)3 (b) -Ō (c) CI CH3 Br

A: According to IUPAC nomenclature we have to first select the parent chain and have to number then .So…

Q: OH CH,CHCH,CC=CH CH, CH3 Çi C1 CH 3-CH-CH 2-CH-C-CH-CH 2-CH2-OH tH-CH, C1 CH3-CH,-CH;-CH2-NH,

A:

Q: 12, CCI4 CH2-0-C-(CH2)7-CH=CH-(CH2)5CH3 H2, Pt CH-O-C-(CH2)16CH3 3 NaОH ČH2-0-C-(CH2)14CH3 H30*

A: The given reactions are :

Q: k H3C-CH2-CH2-C-CH2-ċ-CH3 IUPAC 1. OH IUPAC OH Common Name OH H3C-CH2-CH-CH2-C-H m. IUPAC OH…

A: Applying concept of IUPAC nomenclature of organic molecules we can determine IUPAC nomenclature of…

Q: CH;CH,CH,CH,CH3, CH3CH2CH2CH3, CH;CH2CH3 b. CH¿CH,CH½CH(CH3)2, CH3(CH),CH3, (CH3)½CHCH(CH3)2 a.

A: The temperature  at which vapour pressure of a liquid becomes equal to it's atmospheric pressure is…

Q: CH3 ●• Mg :ÕH :0: || CI CH3-CH,-C-CH3 CH3-CH,-C-CH3 2 H* CH3 :0: || CH3-CH2-C-CH3 CH3-CH,-C-CH3 OCH3…

A: Carbonyl compounds reacts with alkylated magnesium halides (Grignard reagent) and undergo…

Q: 1. CH3-C=CH2 CH3-CH- CH CH3 2. CH3 - CH2 - C=CCH2 -CH; 3. (CH)»CHC CCH(CH)a 4. (CH3):CCH=CCH(CHs)2…

A: Answer  Common name :- old derived and popular name called Common…

Q: What stereoisomers are obtained from each of the following reactions?

A: Since you have posted multiple sub-parts, we are entitled to answer the first three only.

Q: d.-COOH, -CH, OH, -H, -CHO e-CI, -CH,.-SH, -OH (-C=CH, -CH(CH,)2. -CH2CH3. -CH-CH,

A: Given: D. -COOH, CH2OH,-H,-CHO E. -Cl, -CH3,-SH, -OH F. -CCH, -CH(CH3)2, -CH2CH3, -CH=CH2 To find:…

Q: 10 CH 3 CH3 CH3 - CH CH-CH3 CH,-CH- Cェー CH3 10

A:

Q: d. C,H-C-CH, H* e. C,Hs-C-CH f. C,Hs-C-CH; NaOH g. CH;-C=C-CH, HgSO., 4 h. C.Hs-C-C.H,

A:

Q: H3C-CH2 CH3 CH3 2 1 H3C- -CH3 CH2 CH CH2 CH2 H3C CH2 CH3 CH2 H3C CH3 CH3 CH 3 CH 4 Н- -CH3 CHa -OH

A: This question belongs to the rules given by IUPAC for the nomenclature of the following organic…

Q: H2SO4 CH;CHCH2OH CH3 H2SO4 2 CH,CHCHCH,CH3 CH3 Majo CHaCH-CHCH3 +2KOH Br Br

A: ->H2SO4 is a dehydrating agent which form alkene. ->Alco KOH is used for elimination reaction.…

Q: 1) NaBH4 2) CH,CH,ОH OCH2CH3 (А) (В) CH2OH OCH,CH3 ОН (С) ОН (D) .CH2OH OCH2CH3

A:

Q: a. CH;(CH2)4I, CH3(CH2)5I, CH3(CH2)çI b. CH3CH¿CH;NH2, (CH3);N, CH3CH¿CH,CH3 c. (CH3);COC(CH)a,…

A: Boiling point of a chemical compound is the temperature at which vapor pressure of a compound…

Q: Draw curved arrows to show the movement of the electrons as one (or more)bond breaks and another…

A: a. Carbon-carbon π bond undergoes homolytic cleavage. Among the two electrons of carbon carbon π…

Q: Give the complete IUPAC name for each of the following compounds:

A: IUPAC name of (a) Butan-2-ol  IUPAC name of (b) 2-iodo-3,3-dimethylpentan-2-ol  IUPAC name of (c)…

Q: H2N-CHO-OH CH2 H2N-CHC-OH CH2 CH2 H2N-CHC-OH H. C=0 NH2 CHa

A: Given: Different- different structure of amino acids. To find: Common name of amino acids. Solution:…

Q: CI d. CH-CH,-C-CH,-CH CH2 CH3

A: Organic compounds are named according to the rules and recommendation of IUPAC and the names…

Q: How can 1H NMR distinguish between the compounds in each of the following pairs?

A: NOTE: Since, we only answer upto three sub-parts, we'll answer the first 3. Please resubmit the…

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.