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A: Chiral center is that carbon which contain four different substituents attached to it.
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Q: Propose starting materials to synthesize the ether shown below.
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Q: The molecule Br₂CHCHCI2 has how many chiral centers? a) 0 b) 4 c) 2 d) 1 e) 3
A: A chiral center is a carbon attached to four different groups.
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Q: 1. Please write out a possible Slater Determinant for the ground state of lithium atom?
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what would a detailed step-by-step mechanism be for a reaction between bromine and trans-stilbene if the solvent, ethanol, is a stronger nucleophile than the bromide ions?
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- Nucleophilic carbon atoms are often important in the formation of carbon–carbon bonds. Carbon atoms are not good nucleophiles if they do not possess a lone pair of electrons.Write the mechanism, as well as the structure of intermediate A and product B, for the following reaction.Why is benzene a weak nucleophile?
- When propene reacts with gaseous hydrogen bromide, HBr, two products, 1-bromopropane and 2-bromopropane are formed. The reaction is a two-step process in which the electrophilic attack occurs in the first step. Identify the electrophile in this reaction Draw a diagram showing the first step of the reaction that leads to the production of 2-bromopropane.The relative rates of reaction of ethane, toluene, and ethylbenzene with bromine atoms have been measured. The most reactive hydrocarbon undergoes hydrogen atom abstraction a million times faster than does the least reactive one. Arrange these hydrocarbons order of decreasing reactivity.The formate and methoxide ions are both formed by removing a hydrogen atom from a corresponding neutral compound. Given that each process involves the breaking of an O-H bond, explain why the formate ion is so much more stable than the methoxide ion.
- What explains why many aldehydes and ketones can undergo self-condensation reactions in basic conditions? The alpha carbon can lose a proton and act like a nucleophile and the carbonyl carbon is an electrophile. The alpha carbon can gain a proton and act like an electrophile and the carbonyl carbon is a nucleophile. The oxygen of the carbonyl group can attack the carbon of the carbonyl group. Only esters can undergo self-condensation reactions.what will be the type of interaction of ethane with bromine: a) radicals b) ionic c) nucleophilic d) electrophilicBulky, nonnucleophilic bases favor elimination over substitution. Define this ?
- Define nucleophilic aromatic substitution ?1) Nucleophilic substitution reaction of alkyl halide is a process when nucleophile replace the leaving group of alkyl halide. Propose the mechanism and product(s) for the following substitution reaction.What is the product of the reaction of bromoethane with each of the following nucleophiles?