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Q: 3) Please predict the structure of the following molecules with the information you are given A)…

A: Given chemical formula: C3H6O2

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Q: oni. 3. r MgBr a. 1. 2. H20 1. Zeq. a My Br HzO

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Q: Which of the following is NOT a measure of central tendency? a) Mean b) Median c) Variance d) Mode

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A:

Q: HO H Drawing 1. CH3CH₂Li 2. H3O+

A: Given that, the reaction is:

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A: Activation energy is amount of energy required to activate the reactant molecules from ground state.

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Q: а. (еxcess) H3O* b. С. H2O ОН ZI + エーZ

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Q: 12. Calculate % difference using equation 2. Show set-up. |trail 1 density - trial 2 density 0.961 -…

A: Given the trial-1 density = 0.961  Trial-2 density = 0.979

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.