haloalkanes are formed when any halogen get attached to any hydrocarbon chain containing only single bond replacing hydrogen bond
Haloarenes are less reactive than haloalkanes towards nucleophilic substitution reactions because the aromaticity of the benzene ring in haloarenes provides extra stability to the molecule. This stability reduces the likelihood of breaking the aromaticity of the ring during the substitution reaction. In contrast, haloalkanes do not possess this extra stabilization, making them more prone to undergo nucleophilic substitution reactions.
haloarenes are less reactive than haloalkanes because: 1. resonance effect more the resonatinsg structures,more the stability 2.difference in hybridisation of the C-X bond i.e.,in haloalkanes,the hybridisation is sp3 whereas in haloarenes it is sp2 hybridised.As sp2 is more electronegative therefore bond length is shorter and hence stronger. these are the major reasons.
In a primary haloalkane, the carbon involved in the halogen-carbon bond is bonded to one other carbon. In a secondary haloalkane, the carbon involved in the halogen-carbon bond is also bonded to two other carbons.
No, alkanes do not conduct electricity since they are non-polar and do not contain any charged particles that can carry an electric current. Haloalkanes may conduct electricity, but only when they are dissolved in a solvent that can dissociate the halogen atom from the carbon chain, creating charged particles that can carry the current.
Haloarenes are less reactive towards electrophiles than benzene because the halogen substituents on the aromatic ring act as electron-withdrawing groups, reducing the electron density on the ring and making it less susceptible to attack by electrophiles. This results in a decreased reactivity towards electrophilic substitution reactions compared to benzene.
Haloalkanes react with KCN to form nitriles because CN- acts as a nucleophile attacking the carbon of the halogen atom, leading to substitution. On the other hand, with AgCN, the reaction proceeds through an isocyanide intermediate due to the ability of Ag+ to stabilize the cyanide ion, promoting nucleophilic addition to the carbon of the halogen atom.
E2 reaction is expected for secondary haloalkanes with sterically hindered strong bases. This is because the strong base can readily abstract a proton from the beta position, leading to the elimination of the leaving group and formation of the alkene product.
When a metal reacts with a haloalkane it forms an organometallic reagent such as Alkyllithium (RLi) or the Grignard Reagent (RMgX) where R is an alkane and X is a halogen.
Because they have been reacted with primary sulfonate under typical SN2 condition.
Aldo Tomasi has written: 'The metabolism of some haloalkanes to free radical intermediates studied by electron spin resonance spectroscopy andthe spin trapping technique'
Because the +R effect of the haloarene, tends to oppose the -I effect, and hence the deactivation is lesser at the ortho and para positions, compared to any other position (like the meta position). So they tend to be o-p directing.
When fluorine, chlorine, bromine, or iodine atoms are substituted for hydrogen atoms in alkanes, they are called alkyl halides or haloalkanes. These compounds have a halogen atom attached to a carbon atom in the alkane chain.