Question 2: draw structures for the following (a)  ethanol (b)  2-propanol (c)  2-ethyl-5-methylcyclohexanol

Q: (c) H3C-CH-CH-CH3 H3C H₂C-CH3 2-Ethyl-3-methylbutane Spell out the full name of the compound.

A: Given that, the structure of the compound is:

Q: Name this molecule, (a) Propanal (b) Propanone (c) Propanol (d) Propanoic acid 요. CH-CH₂CH

A: IUPAC Nomenclature consists of:Prefix + Root Word + SuffixPrefix denotes branches or secondary…

Q: Draw the structure (wedge diagram) for (R)-3-chloro-2-methylheptane.

A:

Q: Question 1 One of these alkenes shows cis-trans isomerism. Draw structural formulas for both…

A: In this question the they have been asked to draw a cis and trans isomer, the following step…

Q: solve the question: Nmae the following organic compound (Iupac name)

A: The objective of the question is to find the IUPAC name of the given organic compound. The IUPAC…

Q: Give the IUPAC names of structures containing two carbon atoms for the following classes of…

A:

Q: Write structural formulas for the following compounds (includes both old- and new-style names).(a)…

A: Structural formula It is graphical representation of the molecular structure how atoms are possible…

Q: Question 33 Structural formulae of selected alkanes are given here. Rank them in order of decreasing…

A: -> Boiling point of alkanes increases with increasing number of carbons .  -> As the branching…

Q: The following name given is incorrect or incomplete, but it represents a real structure. Draw…

A: The structure of the 3-isopropylhexane is represented as follows,

Q: Q2: Write down the distinguishing features among the following: (a) 10 , 2 0 , 3 0 , alcohols (b) 10…

A: Answer (a): The test is based upon the distinguish between in reactivity of primary, secondary and…

Q: (a) (b) (c) 2-ethylpropylcyclohexane 2,3-diethylhexane 2,3-dimethyl-3-propylpentane

A: Given : incorrect names  Tip: first draw structure then write name

Q: Draw the line formulas for the two molecules. (b) (trans)-1-bromo-2-(1,1-dimethylethyl) cyclobutane…

A: The line angle formula of a compound represent the carbon at the each terminal and joining of two…

Q: Draw structures of the following compounds: (a) 2-methylbenzoic acid (b)…

A: The given names are of that of aromatic organic compounds. The structures are drawn in the next…

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.