21. Which of these is the major product of the reaction conditions shown? Bubble in your answer completely. D H2, Pd/C D

Q: Draw the major product obtained from the following reaction. 1 mol Br₂

A: Bromination of alkene is an electrophilic addition reaction. The reaction proceeds through formation…

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A:

Q: (d) For the reaction 2 NO + O2 → 2 NO2, how many moles of NO are needed to produce exactly 0.500…

A: moles of NO2 = 0.500 molesmoles of NO required =?

Q: 0 CH3 p blob (formate) Heat CH: CHC-0-CH-CH + NaOH (methyl ethyl propanoate)

A:

Q: H3CO OH 2 HCONH2

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Q: 37. Complete the following reaction: CH₂CH H + H₂O/H*

A: The objective of the question is to predict the product formed in the following reaction given.

Q: A chemical reaction is carried out in a se of win J. 0-464J ○ 458J ○ 230 J 0-230 J

A: Initial volume= 1.78 L Final volume= 3.19 L Pressure= 3.25 atm

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Q: provide mechanism

A: We have to predict the mechanism.

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A: The expression to calculate the enantiomeric excess (%ee) can be represented as follows-

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A: Reaction: 1.  luciferin + O2 ⇌   oxyluciferin + light2. . ATP ⇌ AMP+ PPi      Overall

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Q: Complete synthesis, show reagents and intermediate compounds.

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Q: Consider the titration of 110.0 mL analyte solution containing 0.12 mol L-1 NH3 with 0.30 mol L-1…

A: pKb  = - log Kb            =  - log (1.80  * 10-5 )          = 4.745pKa = 14-pKb       = 14- 4.745…

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A: Answer below this question Explanation:

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Q: Draw products and the mechanisms for each of the following:

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A:

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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.