Answer:
The answer is quartet 2.40 ppm.
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Explanation:
Solution
Multiplicity or (n+1) rule:
It helps in determination of multiplicity of an individual proton or individual types of proton which are available in the molecule.
Multiplicity =(n+1)
Thus
The non equivalent protons which are attached from adjacent atom is denoted by n.
Now because there are three non-equivalent protons are present at adjacent carbon of methylene group, hence the multiplicity of methylene hydrogen is given as follows:
The multiplicity will be the same for the two hydrogen's. thus we compute multiplicity only for one hydrogen atom stated below:
Non- equivalent = 3
Multiplicity = (3 +1)
= 4
= Quartet for 2H
A quartet for 2H indicates that the hydrogen atoms attached from the carbon, which is attached one side from a methyl group and the other side form an atom that have no any hydrogens.
Now due +I effect of carbonyl group, chemical shift value is high for these two hydrogens which is exactly at 2.40 ppm or 2.40 Quartet.
Explanation:
the molar mass of the compound is 1502g/mol
Did you have any choices??
Answer:
a. electrophilic aromatic substitution
b. nucleophilic aromatic substitution
c. nucleophilic aromatic substitution
d. electrophilic aromatic substitution
e. nucleophilic aromatic substitution
f. electrophilic aromatic substitution
Explanation:
Electrophilic aromatic substitution is a type of chemical reaction where a hydrogen atom or a functional group that is attached to the aromatic ring is replaced by an electrophile. Electrophilic aromatic substitutions can be classified into five classes: 1-Halogenation: is the replacement of one or more hydrogen (H) atoms in an organic compound by a halogen such as, for example, bromine (bromination), chlorine (chlorination), etc; 2- Nitration: the replacement of H with a nitrate group (NO2); 3-Sulfonation: the replacement of H with a bisulfite (SO3H); 4-Friedel-CraftsAlkylation: the replacement of H with an alkyl group (R), and 5-Friedel-Crafts Acylation: the replacement of H with an acyl group (RCO). For example, the Benzene undergoes electrophilic substitution to produce a wide range of chemical compounds (chlorobenzene, nitrobenzene, benzene sulfonic acid, etc).
A nucleophilic aromatic substitution is a type of chemical reaction where an electron-rich nucleophile displaces a leaving group (for example, a halide on the aromatic ring). There are six types of nucleophilic substitution mechanisms: 1-the SNAr (addition-elimination) mechanism, whose name is due to the Hughes-Ingold symbol ''SN' and a unimolecular mechanism; 2-the SN1 reaction that produces diazonium salts 3-the benzyne mechanism that produce highly reactive species (including benzyne) derived from the aromatic ring by the replacement of two substituents; 4-the free radical SRN1 mechanism where a substituent on the aromatic ring is displaced by a nucleophile with the formation of intermediary free radical species; 5-the ANRORC (Addition of the Nucleophile, Ring Opening, and Ring Closure) mechanism, involved in reactions of metal amide nucleophiles and substituted pyrimidines; and 6-the Vicarious nucleophilic substitution, where a nucleophile displaces an H atom on the aromatic ring but without leaving groups (such as, for example, halogen substituents).
