Br Br Br 3-bromoprop-1-ene (allyl bromide) 1-bromobutane 1-chlorobutane 3-bromo-2-methylprop-1-ene Br Br Br 2-bromobutane 2-chlorobutane benzyl bromide 1-bromo-3-methylbut-2-ene

Q: .CO2H N-H + `NH2 CO2H

A: In this question, we have to find out the correct answer of given problem by the help of the…

Q: 1. What are products of the following reaction: CH-0-Ö-(CH,)16CH3 CH-OH A.) CH-o-C-(CH2) 16CH3 +3…

A: (a) The given reaction is, This is saponification reaction. In saponification reaction,…

Q: H A) (Z)-2,3,6-trimethyl-2-heptene B) (Z)-2,3,6-trimethyl-3-heptene C) (E)-2,3,6-trimethyl-3-heptene…

A: No

Q: Name the following compounds: CH Hex ane a) HạC CH3 CH2 CH2 -CH3 1- PropyI -6 - butYICYclononene H3C…

A:

Q: What is the name of this compound ? .CH2-C=C-CH3 a) 3-butyl-1,3-hexadiene-5-yne b)…

A:

Q: Cl - CH – CH - CH2 – CH, – CH, – CH2 – CH, – CH3 H,0 CH3 O 1-Cyclohexyl-2-methyl-octan-1-ol O…

A:

Q: Give a systematic or common name for each compound. a. CH,NHCH;CH,CH,CH3 e. (CgHs)2NH h. CH,CH3 NH2…

A: Hi, since you have posted questions that has multiple subparts. We will answer the first three…

Q: Br What is the correct name of this compound ? a) 5-bromo-1-ethylcyclohexene b)…

A: Rules for Naming cycloalkenes :-  The double bond of cycloalkene must be given number 1 and 2  If…

Q: Which of the following molecules is non-aromatic? A. 1,3,5-cycloheptatrienyl cation B.…

A:

Q: 3-methyl but-3-enal 3-tert-butylcyclohexane carbaldehyde Acetaldehyde Acetone hex-4-en-2-one…

A:

Q: Which of the following is a primary alkyl halide? (CH3)½CHCHCICH3 (CH3)2CHCH2CCI(CH3)2 O…

A: From  alkane when one or more hydrogen atom is replaced by halogens then compounds obtained is known…

Q: 1. Starting from 1-bromoethane, synthesize ethanenitrile Br CH3CEN 1-bromoethane ethanenitrile 2.…

A: The synthesize of butanamide from ethyne has to be explained.

Q: Show how hex-1-yne might be converted to(a) 1,2-dichlorohex-1-ene. (b) 1-bromohex-1-ene.(c)…

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

Q: 12 & 1.4-addition products from ether cleav Br HBr 2 HI Br Cl,2) (c) (d) OH (1) Na H2SO4 (2) C2H5-Br…

A: In Williamson ether synthesis method, a metal alkoxide ion undergoes reaction with primary alkyl…

Q: Show how hex-1-yne might be converted to(a) 1,2-dichlorohex-1-ene. (b) 1-bromohex-1-ene.(c)…

A: (a) The conversion of hex-1-yne might be converted to 1,2-dichlorohex-1-ene can be shown as follows,

Q: Br2 hv

A: Bromination of alkanes in the presence of hv takes place via a free radical mechanism. It is a…

Q: What is the name of this molecule? (look at the picture to be able to answer) a) (Z)…

A: The absolute stereochemistry of alkenes is preferably described by EZ- nomenclature. If the same…

Q: 2. & ((A) (C) i + CH3 -C-H KOH A & i CH, - CH, - C – CH, – CHO major product: CH = CH₂ (B) (D) CH₂-…

A: Here the driving force for the reaction is to get relief from the bond starain that occurs in three…

Q: What is the appropriate systematic name for the compound below?…

A:

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

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

Q: What is an appropriate systematic name for the following? OH…

A:

Q: f. 2-ethyl-cyclopentane-1,3- dicarbaldehyde g. 2-chloro-3-hydroxy-4-oxo-pentanal h.…

A:

Q: What is the IUPAC name of the compound below? Br Br (E)-4-bromo-5-cyclopropyl-3-hexenoyl bromide O…

A: In order to write iupac nomenclature we have to follow some rules of iupac  1) first select longest…

Q: O (E)-1-chloro-1,2,3-trimethyl-1-butene O (Z)-1-chloro-1,2,3-trimethyl-1-butene O…

A: Given : Structure containing double bond and Chlorine  To find : IUPAC name

Q: .Br CH3 CH3 1S,2S)-1-bromo-1,2-dimethylcyclohexane Rx de B- Eliminación CH 1,2-dimethylcyclohex-1…

A: β-Elimination is a chemical reaction where atoms or groups are lost from adjacent atoms and it…

Q: What is an appropriate systematic name for the following? (Z)-4,4-dimethylhept-2-ene-5-yne O…

A:

Q: Draw the products of the following reactions. If the products can exist as stereoisomers show what…

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

Q: Draw the structures, and show steriochemistry when applicable   1.(S)-3-bromoheptanal 2.…

A: Rule of IUPAC- 1) Longest chain as parent chain. 2) Numbering start from those side where more prior…

Q: CH HC 4-bromo-3,3-dihydroxypentane 2) 1) OH 1-hydroxy-1,3-eyclobutadiene 3)

A: The following names and structures are as follows :

Q: 6. Methanal (HCHO) 7. Naphthalene (CioHe) 8. Acetanilide (CH;-NHCOCH) 9. Uracil NH Cyclohexane…

A:

Q: propanal 1) 2). pentan-2-one H3C H- C- c-c -C-c-c-c H3C CH3 3,3,6-trimethyl- 4 propylheptanal 3) 4)…

A:

Q: Which of these reactions does not occur? a) b) 0=0 c) NHCHs » & c 9)!.!. -OCH₂ CH₂OH ª)ča d) -CI…

A:

Q: The major product from the reaction of HBr with 2-methyl-2-hexene is O 2-Bromo-2-methylhexane O…

A: Nucleophiles such as Bromine ion can add to double bonds under acidic conditions.  When…

Q: (Hydrogenation): 3,3-dimethylcyclopentene + H2 – (hydrohalogenation reaction): 2,4-dimethyl-3-hexene…

A:

Q: What is the best IUPAC (systematic name) for the following compound? Br O…

A:

Q: 7-sec-butyl-4-ethyl-3-decene O 4-ethyl-8-methyl-7-propyl-3-decene O…

A:

Q: 4-bromo-3-ethyl-5-methylcyclohexanone H;C-H2C- b) H;C- а) Br Br ČH2-CH3 ČH3 H;C-H2C- d) Br c) Br CH3…

A:

Q: (S)-3-methyl-1-penten-4-yne; f. (3S,8S)-8-chloro-3,8-dimethyl-5-decyn-3-ol e. g.…

A: Structure of given compounds can be drawn by following IUPAC nomenclature rules.

Q: 1. Starting from 1-bromoethane, synthesize ethanenitrile Br CH,CEN 1-bromoethane ethanenitrile 2.…

A:

Q: Pick the best IUPAC name for the following molecule: Cl- OH F 1-chloro-6-fluorocyclohexan-3-ol…

A: In the above compound alcohol is the primary functional group.

Q: (b) 1-methyl -3-chloro-4-lodo Cyclo pentane (C) 1- Chloro-2-lodo-4-methyl Cyclo pentane (d)…

A: The question is  based on concept of IUPAC NAMING of organic compounds. There are certain rules to…

Q: C. 1) 1-bromocyclohexane sodium ethoxide 2) H30 d. 1) 1-bromocyclohexane LDA 2) H,0°

A:

Q: ÕH (2S,6Z)-6-ethyloct-6-en-2-ol O (2R,6E)-6-ethyloct-6-en-2-ol O (2R,6Z)-6-ethyloct-6-en-2-ol…

A: Provide the systematic name for the following structure according to IUPAC rules:

Q: What is the best name for the following molecule CH3 -CH3 CH3 O (2E) 4-ethyloct-2-en-6-yne O (6Z)…

A: IUPAC rule, 1. Longest chain as parent chain. 2. Numbering start from those side, where substituent…

Q: NAME STRUCTURE 1 1-bromobutane Br 2 Bromobenzene Br 3 2-bromobutane Br 4. 1-chlorobutane CI…

A: SN1 : It involves carbocation formation. Hence, greater is the stability of intermediate…

Q: What product is formed when But-1-yne is treated with excess of HBr?   1,2-Dibromobutane…

A:

Q: 4-tert-butylhexa Methanol Sodium Cis/Trans- 4-tert-butylcyclo hexanol ne Borohydride H 18 CH OH Mol.…

A: Theoretical yield is calculated from balanced chemical equation. For this we need the number of…

Q: Reaction between CH3OCH3 and H2NCH; will give the following compound. (a) CH;OCH,CH;NH2 (b)…

A: The reactant species are dimethylether and methylamine. When the given reactant react together their…

Q: 0-4 Br Br A. 1-hydroxy-2,4,6-nitrobenzene B. 2,4,6-tribromophenol C. 2,4,6-bromohydroxybenzene D.…

A: In iupac nomenclature, firsr we select the parent long carbon chain which includes main functional…

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.