The structure for the given formula has to be determined under given condition. Concept Introduction: IR spectral studies: It is a spectroscopic technique which is used to determine the functional groups present in the given compound sample by absorbing frequency in particular range with respect to the group present in the given sample. 1H NMR: A technique gives information to predict the Carbon and Hydrogen connectivity in the organic compounds. HDI (Index of hydrogen deficiency): HDI values gives information on the level of unsaturation (means a double bond or a ring) on the structure of the compound. HDI= ( 2C+2+N-H-X ) 2 C indicates number of carbon N indicates number of nitrogen H indicates number of hydrogen X indicates number of halogen Molecular formula: It represents the types of atoms with their total number present in a given molecule.

Question

Want to see the full answer?

Answer 1

Question

Chapter 14, Problem 56PP

Interpretation Introduction

Interpretation: The structure for the given formula has to be determined under given condition.

Concept Introduction:

IR spectral studies: It is a spectroscopic technique which is used to determine the functional groups present in the given compound sample by absorbing frequency in particular range with respect to the group present in the given sample.

1H NMR: A technique gives information to predict the Carbon and Hydrogen connectivity in the organic compounds.

HDI (Index of hydrogen deficiency): HDI values gives information on the level of unsaturation (means a double bond or a ring) on the structure of the compound.

HDI= ( 2C+2+N-H-X)2

C indicates number of carbonN indicates number of nitrogenH indicates number of hydrogenX indicates number of halogen

Molecular formula: It represents the types of atoms with their total number present in a given molecule.

Expert Solution & Answer

Want to see the full answer?

Check out a sample textbook solution

See solution

Students have asked these similar questions

Protecting Groups and Carbonyls 6) The synthesis generates allethrolone that exhibits high insect toxicity but low mammalian toxicity. They are used in pet shampoo, human lice shampoo, and industrial sprays for insects and mosquitos. Propose detailed mechanistic steps to generate the allethrolone label the different types of reagents (Grignard, acid/base protonation, acid/base deprotonation, reduction, oxidation, witting, aldol condensation, Robinson annulation, etc.) III + VI HS HS H+ CH,CH,Li III I II IV CI + P(Ph)3 V ༼ Hint: no strong base added VI S VII IX HO VIII -MgBr HgCl2,HgO HO. isomerization aqeuous solution H,SO, ༽༽༤༽༽ X MeOH Hint: enhances selectivity for reaction at the S X ☑

Draw the complete mechanism for the acid-catalyzed hydration of this alkene. esc 田 Explanation Check 1 888 Q A slock Add/Remove step Q F4 F5 F6 A བྲA F7 $ % 5 @ 4 2 3 & 6 87 Click and drag to start drawing a structure. © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Ce W E R T Y U S D LL G H IK DD 요 F8 F9 F10 F1 * ( 8 9 0 O P J K L Z X C V B N M H He command

Explanation Check F1 H₂O H₂ Pd 1) MCPBA 2) H3O+ 1) Hg(OAc)2, H₂O 2) NaBH4 OH CI OH OH OH hydration halohydrin formation addition halogenation hydrogenation inhalation hydrogenation hydration ☐ halohydrin formation addition halogenation formation chelation hydrogenation halohydrin formation substitution hydration halogenation addition Ohalohydrin formation subtraction halogenation addition hydrogenation hydration F2 80 F3 σ F4 F5 F6 1 ! 2 # 3 $ 4 % 05 Q W & Å © 2025 McGraw Hill LLC. All Rights Reserved. F7 F8 ( 6 7 8 9 LU E R T Y U A F9