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Many chemical reactions are favored by heat.
My guess would be that Elimination reactions are much higher energy, as it breaks bonds. Higher temperature = higher energy.
Stereo-selective addition reactions commonly yield Diastereomers. The major product will result in the one with less steric tension. That is, if a product with two *C is made from a reactant which had 1 *C, then the erythro form would be its major form; electron-rich substituents are more stabilized.
1. Explain with suitable examples: a) Both chlorobenzene and chloroethene do not undergo substitution reactions under ordinary conditions with NaOH. b) Carbonyl group of benzaldehyde is less reactive towards nucleophilic addition reactions than the carbonyl group of ethanal. 2. Write the product (s) and mechanism for the following reactions: (5) 3. How would you carry out following conversions? a) Ethene to oxirane b) Benzyl magnesium chloride to 3-phenylpropanol c) Propene to glycerol d) Benzaldehyde to 3-phenylpropenoic acid e) Ethanol to trichloromethane (5) 4. a) How would you differentiate between different classes of alcohols? b) Give two reduction methods which can convert a carbonyl compound to an alkane.
CO(g)+3H2(g)->CH4(g)+H2O(g)
aniline would go through an electrophilic substitution, it is a weak base
As posed, the question makes no sense on several levels. Benzene is not saturated although it is far less reactive than would be expected for an unsaturated compound due to delocalisation of the electrons. I am unsure what you mean by asking if saturation and "unsaturation" are the same.
Many chemical reactions are favored by heat.
My guess would be that Elimination reactions are much higher energy, as it breaks bonds. Higher temperature = higher energy.
C6H12 is a tetahedral since c will be your central atom and your atom would have four bonds not three
No, it is not valid to conclude that the addition of a base would slow down a reaction.
Three types of gene mutations are substitution, insertion, and deletion. Another gene mutation would be frame shift. All these mutations can cause deformities of the gene.
Substitution can occur in a great many different situations. Substitution usually occurs when someone is scheduled to teach for example and becomes sick.
For nonpolar substances, anything that is symmetrical is nonpolar, so something likeHexane (C6H12) or any other hydrocarbon would work.
Stereo-selective addition reactions commonly yield Diastereomers. The major product will result in the one with less steric tension. That is, if a product with two *C is made from a reactant which had 1 *C, then the erythro form would be its major form; electron-rich substituents are more stabilized.
That would be a substitution
exon