(a). (b). (c). 5. Complete the following syntheses. H—H + H- H-H -CH3 H—=H H. OH H

Q: NABH4 CH3 COCH2CH3 CH;CH2OH

A: No reaction, NaBH4 is not strong as to reduced ester compound into alcohol.

Q: 16. Draw significant resonance structures for the following compound. Which of this is/are most…

A: When all the properties of a molecule cannot be explained by a single structure , we draw more than…

Q: CH2 H3C H3C COOH Reagents e. PB13 f. NaCN then H3O* g. NBS, CCI4 h. CrO3, H2SO4 а. HBr b. Mg, ether…

A:

Q: Give the IUPAC names for all of the following compounds. Indicate (R) or (S) configuration for the…

A:

Q: Give the product

A: In the first reaction, the reactant reacts with magnesium metal to form Grignard reagent, which…

Q: HgSO4 H2SO4, H2O 1T (1) Br Вн, THF H,Oг, NaOH 10 NANH2 H =H 1S NH3 H20 HCI (1 equiv.) diethyl ether…

A: NaNH2 abstracts the acidic hydrogen from alkyne which reacts with alkyl halide to gives alkyne (1S).…

Q: W W 21 - Su2... G b Provide the systematic (IUPAC) name for each of the following saturated…

A:

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: `NH2. KOBR 2. НО (A) >(B). Compound (B) is : :- NH- (a) -NH – Ĉ – H (b) - CH3 (c) -NH- (d) Oʻ -NH2

A: In the given reaction the reactant contains an amide and a carboxylic acid functional group. The…

Q: Which of the following best describes why only small aldehydes and ketones are soluble in water? A)…

A: Aldehydes and ketones are organic molecules with a carbonyl group, i.e. a double bond between carbon…

Q: 2.) Cyclohexane Why insoluble in water? Why insoluble in HCl? Why insoluble in NaOH? Why insoluble…

A: The answer of the above question is given in step 2

Q: The alkyl group (CH3)2CH- is a(n). group. (a) tert-butyl (b) iso-butyl (c) n-butyl (d) sec-butyl (e)…

A: Two compounds having similar molecular formula but distinct structural/bonding arrangements of atoms…

Q: Alcohols & Ethers 1. Name the following Alcohol and Ether: OH CH3 (a) CH3-CH-CH2-CH-CH-CH2-CH3 (b)…

A: Write name of alcohol and ether and draw structure for the given name ---

Q: (b) H H CH2CH3 ·C. -CH2CH3 CH3 CH3OH (H)

A: The methanolysis of a tertiary alkyl halide involves the substitution of the halogen atom (usually a…

Q: Write the IUPAC names of the following compounds. CH;CH(C,H;)CH(CI)CH(OC,H;)CH(C,H;)CH; 2.…

A: Given compounds:

Q: 1. Write bond-line formulas for (a.) four aldehydes with the formula of C5H10O (b) three ketones…

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

Q: What is(are) the major Organic product(s) in the following reaction? CH; CH; (a) CH; H₂C-C-0-CH;…

A:

Q: Julie has been asked to measure the concentration of a sample solution using a spectrophotometer.…

A: On dilution, the no of moles does not change. As no of moles = Molarity × Volume Thus, (Molarity ×…

Q: Which of the following structures have the lowest boiling point? a. (CH3)3-C-CH2-CH2-CH3 b.…

A: Hydrogen bonding of organic compounds depends on many intermolecular forces of attraction likeVander…

Q: 1. Give the IUPAC names of the following compounds. (a) (b) F & Br CI (c) (d) O₂N. CH3 CH3

A:

Q: oto 1)NaOEt/H₂O 2) H₂O+ ?

A: Given is organic reaction. The name of given reaction is Favorskii rearrangement. It is reaction of…

Q: Identify the class of the compound based on its functional groups. H3C *CH3 H3C° H. (b) alcohol…

A:

Q: Alkene reactant Products Name of the product (CH,),C=CHCH,CH,CH, + HCI CH CH, + H,0 4SO.. CH OH +…

A: Since, this is a multiple subparts questions. So, I will solved in details first three subparts for…

Q: Give the IUPAC names of the following alcohols. CH, HO OH `CH, (а) (b) Br ỌH CH (с) (d) HO ČH,…

A: The IUPAC name is given as follows

Q: 1. Give the IUPAC names for the following alcohols. (а) ОН OH (Ь) ОН (с) НО CH3CHCH2CHCHCH3…

A: Rules for IUPAC nomenclature:  1) select the longest carbon chain as parent chain. 2) identify the…

Q: 3. Name the following alkynes. (a) (b) CH3CH₂CH₂CH₂CH₂CH₂C = CH CH₁ CH₁ CH₂-CH-CH-CH-CH—C—CH I CH₂…

A: The alkynes bear a triple bond between two carbon atoms. According to the IUPAC nomenclature,  the…

Q: 1. Rank the following molecules and provide a brief explanation. (a) Rank the following in terms of…

A: Rank the following molecule

Q: 1. Which compounds have a carbon-carbon triple bond? 2. Which have an aldehyde or ketone carbonyl…

A: Given compounds are : To solve the questions, we need to know the structure for the different…

Q: 1.) H-B- 2.) H2O2, NaOH (xs) a) b.) d)

A:

Q: Chemistry (c) Benzene (E) is converted to product F by the two-step process detailed below. Draw…

A: In Friedel-Crafts Acylation, Lewis acid and the chlorine atom of the acid chloride create a complex.…

Q: Provide the systematic (IUPAC) name for each of the following saturated hydro (a) (b) H₂ H₂C-C (c)…

A:

Q: The action of heating one mole of water (containing a trace of acid catalyst) on one mole of…

A:

Q: (a) 'CI (b) НО НО (C) F Br ОН

A: Ring is numbered as per IUPAC priority .substituent is selected alphabetically.

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.