Hi,
Hope you are doing well.
__________________________________________________________________________
PART 1:
IUPAC Name: cis-5-octen-2-yne.
STRUCTURE:
__________________________________________________________________________
PART 2:
IUPAC Name: 1-ethynyl-1-methylcyclohexane
STRUCTURE:
__________________________________________________________________________
PART 3:
IUPAC Name: (2,2-dimethylbut-3-yn-1-yl)cyclopropane
STRUCTURE:
If you need help in numbering,
please let me know.
__________________________________________________________________________
Hope this helped for your studies. Keep learning. Have a good day.
Feel free to clear any doubts at the comment section.
Please don't forget to give a thumps
up.
Thank you. :)
1. Draw: CIS-5-OCTEN-2-YNE 2. Name the structure 3. Name the structure
Draw the Halogenation of avenges c arrow push give the structure of (6z) - 6methyl-6-octen-1-yne draw the keto-enol forms of the ff compounds in process of acid E^1_1 base Draw mechanism and possible products.
Help please Draw the following alkynes: 4-bromo-3, 3-diethylhex-i-en-5-yne 3, 10-dimethy-6-secbutylcyclodecyne) 1, 3-hexadien-5-yne s-ethyl-s-methyl-1.6.8-decatriyne Z-5, 7-dimethyl-4-octen-1-yne
1. Draw the structures of: a) (Z) 2-iodo-3-methyl-2-heptene b) cis non-3-en-5 yne Give the IUPAC name of the following compounds, including steochemistry. a) F CH2CH2Br CH3CE 2. a) Draw the most stable chair conformation of cis 1,3-difluorocyclohexane. b) Draw a Newman projection of 2-iodo-3-methylpentane looking down the 3. Compound X has the formula CoHB2Br4. Compound X reacts with excess H2/Pd to give CATHa6Bra. How many does compound X have? Show how you got your answer. rings 4. For each pair...
4. CH CHCH2CH2SH 5. CH 6. H 7. Draw cis-4-octen-2-ol s.Draw 4-hydroxycyclohexanone
Draw the structure of (E)-4-bromo-5-methylhex-3-en-1-yne.
Draw a dash-wedge structure for (R)-5-methylhept-2-yne
1. Name the following compounds using IUPAC or accepted common name: 2. Draw a proper condensed, expanded or line-angle structures for the following compounds: /8 a. hepta-1,4-diyne b. cis-non-2-en-5-yne c. trans-6-chlorohept-2-en-4-yne
2.1. Name the following compound. Specify cis/trans geometry, if applicable. Q.2. Draw line structure for cis-4-methyl-2-hexene. 03. Draw a strucrure with molecular formula CH,20 which exhibits cis/trans isomerism, and also has a chiral center. How many stereoisomers are possible for this molecular formular? Q.4. What is the index of hydrogen deficiency of a compound with molecular formula C-H, BINO? Q.5. How many stereoisomers of 4-chloro-2-pentene exist? a 1 6 . 2 c. 3 d. 4.
Draw the structure of the starting material needed to make 2-methylhept-3-yne using sodium amide in liquid ammonia, followed by 1-bromopropane.
bond line structure of the following compounds on the lines 2. (5 pts.) Name or draw the bond line struc provided: a. (25, 6R)-cis-3-hepten-2,6-diol b. (hint: use R/ S nomenclature in the name) HO