Reactions of Ethyl-3-pentenoate with all given reagents are given below.
Reaction with H₂ / Pd:
The non-polar double bond present in Ethyl-3-pentenoate is reduced to saturated chain. This reagent can not reduce the carbonyl group.
Reaction with NaBH₄: Sodium Borohydride is a weak reducing agent at compared to LiAlH₄. It can only reduce aldehydes and Ketones to corresponding alcohols.
Reaction with LiAlH₄: Lithium Aluminium hydride is a strong reducing agent. It can reduce all types of carbonyl compounds to corresponding alcohols, But, it can not reduce non-polar double bonds like alkenes and alkynes.
Result: The correct answer is
Option-A (Highlighted RED below).
Answer :
The correct answer is %IC = 10 % and bond is covalent bond with slight polarity.
<u>Percent Ionic Character :</u>
It is defined as percent of ionic character present in a polar covalent bond . The formula of % ionic character (%IC) is given as follows :
Where Xa = Electronegativity of A atom and Xb = Electronegativity of B atom
Given : Molecule is TiAl₃
Electronegativity of Ti = 2.0
Electronegativity of Al = 1.6 ( From image shared )
Plug the value in above formula :
Value of e⁻¹ = 0.90
Percent ionic character = 1 - 0.90 * 100
Percent Ionic character = 10 %
<u>Since the % IC is 10 % , which is very less comparatively , hence the bond is covalent and very less polar .</u>
Copper nitrate and nitric oxide are produced in this reaction.
Answer:
12.78 kJ
Explanation:
The correct balanced reaction would be
Mass of methanol = 
Moles of methanol can be obtained by dividing the mass of methanol with its molar mass 
Enthalpy change for the number of moles is given by
The change in enthalpy is 12.78 kJ.
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).
