C3H6 is chemically reactive, because it is Select one: O a. not: saturated O b. very: made of hydrogen and oxygen O c. moderately: made of polarizable carbons d. very: under ring strain O e. not: symmetric Clear my choice

Q: 1. Given below are the structures of five hydrocarbons. 442 H-C-C- H H H H CH3 HHHH H-C-C-C-H H H…

A: Hey, since there are multiple questions posted, we will answer first question. If you want any…

Q: (A, B, or C). Cis and trans isomer will only exist in structure O A. Alkane O B. Cycloalkane OC.…

A: The answer for the following question is -

Q: The dimethylcyclohexane with the structure shown below is: ÇH3 ČH3 Select one: O a. a trans isomer…

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Q: 10) 2 mole 2-methyl cyclopentanone CH3 a) CH3 b) 11) e OH b) ? Na OEt CH3 c) ? & C) CH3 CH3

A: Ist question:  Answer of ist question is (a) , explained with a mechanism.

Q: 2 mehgiheene ..syclohexene. HO H. P-benzoicacid.

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Q: Name the following branched saturated hydrocarbon. 6. 7. H,C- CH- -CH3 H,C-CH2-CH,-CH-CH2-CH2-CH3 8.…

A: The IUPAC nomenclature system is used to give the unique names to the hydrocarbon compounds. As; the…

Q: Draw all the alcohol having the formula C5H12Land which are choral

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Q: + CH3MgBr a.

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Q: Name these organic compounds: structure CH₂ || CH,— CH,−C– CH, CH3 1 CH,—CH— C=CH CH3 | CH3-C=CH -…

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Q: Name each monosubstituted benzene. a. H;C-CH, b. F C. CH3 H;C-C-CH,

A: a) The name of the given mono-substituted benzene is, Ethyl benzene

Q: Which of the following can be used to represent the compound pentane? a) CH,- (CH,), - CH; H. H. H H…

A: 1. Select the principle carbon chain 2. Numbering 3. Naming (prefix + word root + suffix)

Q: 1.) LIAIH, NH 2.) H,O* a.) b.) c.) но. NH NH Racemic d.) e.) но HO,

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Q: CH3 H3C (1) H2 H2 -CH3 H3C (2) fu CH

A: 1.

Q: Draw the structure and give the systematic name for a compound with molecular formula C5H12 that has…

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Q: the balanced equation for the reachion ? itin tinn Cole Late dla

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Q: 4. Name the may be in unusualo conformations.. a. Octane? aribon eaignaind aotcupe esbrin i (ofonia)…

A: Here the structure (A,B,C) are given in ball and stick model.The structure D is a line structure.

Q: Which of the following structural formulas does not have the molecular formula CaH?

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Q: Classify each of the following salts as an amine salt or a quaternary ammonium salt.

A:

Q: 34. Hot and spicy foods contain molecules that stimulate pain-detecting nerve endings. Two such…

A: (a)

Q: only single covalent elect one: O a. alkanes O b. allylenes DC. alkynes O d. alkenes

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Q: Suntnesize the final conm pand belan prom benzene ond any ahe orgonic or incrgchic neagertS Br

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Q: i. h. IN CI j. H3O+ O heat H3O+ 1) LiAl(OR)3H 2) H₂O

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Q: Provide structures of the reactant/products: .cOOEt a) a Na OEt COOE. H,0* b) 1. NaOCH2CH3 2. H30*

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Q: Which statement is incorrect about ?(butene (CH3-CH2-CH=CH2 Z)-But-2-ene is more stable than) O…

A: Solution

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

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Q: I H H HH I: H # H. CH3 Ι H H C. H I ד. H H H CH3 b. a. H H. H H I H H H H H a.

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Q: Draw the skeletal structures for the compounds in a. (Z)-1,3,5-tribromo-2-pentene  b.…

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Q: 4. Draw the following compounds

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Q: Four alkyl groups bonded to carbon marked * in the molecules shown below are: CH3 IV CHCH3 CH3…

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Q: Frange the following compounds in order of increasing boiling point. Clear All CH3CH2CH2C-OH Lowest…

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Q: 10.)(Name the following alkanes (IUPAC names). a.) H-C -H H-C-- H H H HA c-č-č-H b.) с.) H H H H…

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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.