metny4-ethyl-3,3-dicyclopropy-1-hexene is the correct name for which of the following! a. c. HC CH -CH -CH-CH3 H2C CH-CH2CH3 CH Hc CH, CH3 b. d. HC C=CH -C CH-CH2CH CH CH2-CH HOEC HC HC CH CH 2CH 29. 0-CH2-CH, H3C-CH-CH2-CH,-C The correct IUPAC name for the compound above is which of the follow ing? a. 5-o-2-cthy Ipentane ether b. 2-cthoxy-5-pentanone 3-propoxypentanal d. 4-cthoxypentanal с. 30. Which of the follow ing is the correct name for the compound be low? a. benzene-ethanol b. pheny Imethanoate c. methy lbenzenal d. phenyImethanol

Q: h) CH3-CH2-CH2-CH2- ċ=ċ-CH3 i) CH3 -CH3 CH3 CH3-CH,–ĊH ČH3 HIC

A:

Q: 33. What is each compound's systematic name? a. CH₂C=CCH₂CHCH, Br b. CH₂C=CCH₂CHCH, CH₂CH₂CH₂ CH, c.…

A: Steps for naming an organic compound-  1- find the functional group first.  2- determine the longest…

Q: CH3 a. CH;CHČH,CHCH; ČH; CH3 CH3 CH3 b. CH,CCH,CH,CH,CCH3 ČH3 ČH3 c. CH;CH,CHCH,CH,CH,CH3 ČH,CH,CH3…

A: For writing IUPAC names, we need to selecta longest parent carbon chain first. Then we need to check…

Q: CH3-CH-CH₂-CH₂-CH3 and sanit 8. Give the IUPAC name for the following alkanes: CH3 Br…

A:

Q: Give the IUPAC name for each cycloalkane.

A: Since you have posted a question with multiple sub-parts, we will solve first three subparts for…

Q: Draw arrows and all major and minor resonance contributors for the following molecules. Do not…

A:

Q: 4. Name the following compounds: a. CH,CH,CH,CH; CH, CH, M CH3 CH2 ČH2 CH3 b. CH-CH-C C-CH, CH, CH2…

A:

Q: CH, - CH, CH3 - CH, - CH, - CH, - N - CH, - CH, - CH, CH, - CH, - CH, - NH - CH, - CH, CH, - CH, -…

A: The first and the foremost step while naming the IUPAC name of an organic compound is the…

Q: a. b. C. d. F H3C H3C H3C H3C CH 2 CH2CH2CH3 CH -CH. H3C -CH3 CH3 CH CH H2C -CH2 C CH 3 CH 3 CH3 CH₂…

A: a) C-1 is 'R' configuration.C-2 is 'S' configuration.b) This is alkane compound. Long chain contains…

Q: a. CH3CH₂-C=C-CH₂CH₂CH3 ·00 C=C b. c. HC=C–CH,CH,–C=C–CH3 (HO)

A: -> Ozonolysis of Alkyne in presence of water formed carboxylic acid as products. ->pi system…

Q: 12) Which structure is different from the compound (I) ? I CH₂ CH₂- H H a H CH(CH3)2 H. H CH₂ CH₂ H…

A:

Q: What is an i somer of CH =C? CH3 CH's CH3

A: Given:  To find: isomer of the given compound.

Q: 17. Name the following alkynes. b. H H H- H-c=c- H H H. H H d. H-C=c- -CH,-CH, H- C- H H f. CH3 H2C…

A:

Q: A. Name the following compounds according to IUPAC rules CH3 Br CH;CH3 Br OH A

A: IUPAC nomenclature It is a method of naming a particular compound according to international rules

Q: A student drew the structural diagram shown below. CH, 2 HHHHHHHH III 1 H-C-C-C-C-C-C-C-C-H I III…

A: To find the isomers we have to match the chemical formula of the structures with the structural…

Q: 1. The Chemical structure of 5-Bromo-4-Chloro-1- methylcyclohexene is А. Вr CI В. Вг CI С. Вг Br. D.…

A:

Q: Which structure below represents 4-methylpent-2-ene? a. CH3-CH2-CH2-CH2-C=CH2 O b. CH3-CH2-C=CH-CH3…

A:

Q: 1. Provide proper IUPAC names for the following compounds. a. CH3 | CH3C CCHCH2CH2CH3 CH3 Br b.…

A: Step 1: Step 2: Step 3: Step 4:

Q: What is the name of this molecule? Hビーとーとニ( う ょう - C=C 3 ethyl, 3 pentyl 1-nonene OA OB2 ethyl, 4…

A: i) The longest carbon chain in the given molecule has 9 carbon atoms. Therefore, the root word is…

Q: CH,-CH-C= C-CH, 28 The correct IUPAC name for the compound IS Br Da.4.bromopentyne…

A: IUPAC - International union of pure applied chemistry

Q: CH, - CH, - CH,- CH, - CH, - NH, CH, - CH, - CH, - CH, - CH, - CH, - CH, - NH,

A:

Q: CH3 CH3 H3C AICI3 е. CI f. H2C=CH-CH=CH2 (cis) H3C-CH=CH-COOH

A: (e) This reaction is known as "Friedal-Craft alkylation." Because,  benzene is reacting with alkyl…

Designing a Synthesis

Organic synthesis is a branch of chemical synthesis that involves the planned construction of organic compounds/molecules from smaller units that possess functional groups. Friedrich Wöhler was the first scientist who designed the synthesis of an organic compound, urea from inorganic starting materials silver cyanate with ammonium chloride via a simple, one-step synthesis.