a) trans 2,3-epoxy-3-methylpentane
Note :-
In trans isomer bulky or identical groups (or atoms) lie on opposite side of each other.
--------------------------------------------
b)
1-ethoxy-1-methylpropane
Note :-
According to IUPAC system, ethers are considered as derivatives of hydrocarbons in which a hydrogen atom is replaced by -OR or -OAr group.
In mixed ethers, the alkyl group containing larger carbon chain is considered as parent alkane.
-------------------------------------------------
c) 3-methyl-hexen-3-ol
Note :-
Here alcohol (-OH group) is the principal functional group.
------------------------------
Provide structures or names for the molecules below. a) trans 2,3-epoxy-3-methylpentane c) 5-methyl-4-hexen-3-ol
What is the IUPAC name of the following compound? OH (E)-5-methyl-2-hexen-5-ol (Z)-5-methyl-4-hexen-5-ol (E)-2-methyl-4-hexen-2-ol (Z)-2-methyl-4-hexen-2-ol
What is the IUPAC name of the following compound? (Z)-5-methyl-2-hexen-5-ol (Z)-2-methyl-4-hexen-2-01 (E)-5-methyl-2-hexen-5-ol (E)-2-methyl-4-hexen-2-ol
Draw a dash-wedge structure for (S)-3-methyl-5-hexen-3-ol
Give the Line Drawing for the followingg (g) 1-chloro-3-methylbutane (h) pentane (1) 2,3-dichloro-2-methylpentane ) 2-chloro-2,4,4-trimethylpentane(k) trichloromethane ()2-butanol (m) 3-methylpentane (n) 3-bromo-2-methylpentane (o) 3-ethylhexane (p) 5-isopropyl-3-methyloctane (q)3,3-dibromo-1,1,1-trichlorobutane (r) cis-1-bromo-2-pentene (s) 2,5-dimethyl-1-hexene (t) 2,5,5-trimethyl-3-heptyne (u) trans-1,2-dibromo-1-butene (v) 2-ethyl-1-butene (w) 5-bromohept-6-en-3-ol (x) 5-methyl-4-hexen-1-yne (v) 3,3-dimethyl-1-butanol (z) butane
The
reagent options are the same for all boxes
Trans-4-hexen-3-ol can be synthesized starting from acetaldehyde. One of the key reagents is ethyl grignard. Synthesize ethyl grignard from acetaldehyde in the steps below using the reagents provided. Synthesize (trans)-4-hexen-3-ol from acetaldehyde. Select the best reagents and conditions. H_3O^+ PBr_3 Mg, ether NaOH/H_2O, heat PCC Br_2 NaOH, H_2O LiAlH_4
Which compound matches the IR spectrum? 1-hexen-3-ol 1-methylcyclopentene 3-hexanol 1.5-hoxadiene cylohexane trans-4-octene dipropyl ether Which compound matches the IR spectrum? cyclohexane dipropyl ether 1-hexen-3-ol 1.5-hoxadiene 3-hexanol trans-4-octene 1-methylcyclopentene Which compound matches the IR spectrum? dipropyl ether cyclohexane 1.5-hexadiene trans-4-octene 3-hexanol 1-hexen-3-ol 1-methylcyclopentene
What is the systematic name of compound B? (3) OH B (A) (R)-3-butyl-5-hexen-1-ol (B) (R)-4-butyl-1-hexen-6-ol (C) (S)-4-butyl-1-hexen-6-ol (D) (R)-3-allyl-1-heptanol (4) What is the major product of the following reaction? excess HC CI C (A) (B) (C) (D)
Trans-4-hexen-3-ol can be synthesized starting from
acetaldehyde. One of the key reagents is ethyl grignard. 1.
Synthesize ethyl grignard from acetaldehyde in the steps below
using the reagents provided.
Which compound matches the IR spectrum? Dipropyl ether cyclohexane 1, 5-hexadiene 3-hexanol 1-hexen-3-ol trans-4-octene 1-methylcyclopentene
Which compound matches the IR spectrum? 1-methylcyclopentene 1-hexen-3-ol 3-hexanol cyclohexane dipropyl ether 1, 5-hexadiene trans-4-octene